JDTWKLF
JDTWKL
7050 PK
7060 PK
0.7
PLACEMENT WITH RATCHET OR TORQUE WRENCH
NP · RP · WP
JDTORQUE® RATCHET WRENCH
JDTORQUE® TORQUE WRENCH
RATCHET WRENCH ADAPTER
LONG RATCHET WRENCH ADAPTER
IN
Position the ratchet or torque set +
adapter + implant in the implant area.
Insert the implant in the tightening direction Remove the RATCHET OR TORQUE set +
[IN] of the ratchet or torque.
adapter carrier.
WARNINGS
VERIFY THAT THE CONTRA-ANGLE FIXED DRILL FITS CORRECTLY.
DO NOT START THE OPERATION THREAD WITHOUT CHECKING THAT THE RESERVE OF THE DRILL WITH IMPLANT OR
THREAD STARTER IS CORRECT.
OVERCOMING THE TORQUE OF 45 NCM MAY CAUSE DAMAGE TO THE CONTRA-ANGLE AND THE DRILL IF THE
RESISTENCE THAT THE BONE OFFERES GOES OVER THE 45NCM, AND DOES NOT ALLOW THE INSERATION OF THE
IMPLENT ENTIRELY , CONTINUE WITH THE WRENCH RATCHET.
FAILURE TO FOLLOW THE RECOMMENDATIONS OF SURGICAL SEQUENCE CAN CAUSE
DIFFICULTY IN IMPLANT INSERTION, RESULTING IN EXCESSIVE COMPRESSION IN THE IMPLANT AREA. IMPLANT FORCED
INTEGRATION CAN PRODUCE FAILURE
DISASSEMBLING THE CARRIER
To facilitate proper placement of the implant hex connection protecting
the KL implant is presented with a carrier of titanium.
To remove the carrier:
1- Freeze the transporter with the flat rachet [Ref K 7000 A] by
inserting the rachet top to bottom [a].
a
b
c
2- Unscrew the hex connection, either motor or reverse mode with
manual hex 1.2mm adapters [Ref 50 08 04, 50 08 05 or 50 08 06].
[B / c].
WARNINGS
FAILURE TO FOLLOW THE RECOMMENDATIONS OF SURGICAL SEQUENCE CAN CAUSE DIFFICULTY IN IMPLANT
INSERTION.
YOU SHOULD BE AWARE THAT THE RATCHET WRENCH HAS NO CALIBRATION ANY SPECIFIC AND MAY GENERATE
EXCESSIVE FORCE TO DAMAGE THE INTEGRITY OF THE IMPLANT AND INSTRUMENTAL IN ADDITION TO CREATE
ALVEOLAR COMPRESSION EXCESSIVE TO CAUSE BONE NECROSIS AND THEREFORE LOST
SETTING.
IMPLANT FORCED INTEGRATION CAN PRODUCE:
• DAMAGES IN CONNECTION.
• INSTRUMENTAL DAMAGE INDICATED FOR IMPLANT INSERTION.
• COLD WELDING OF SUCH INSTRUMENTAL WITH IMPLANT.
• OSSEOINTEGRATION NON COMPRESSION EXCESSIVE IMPLANT IN BONE
NP COVER SCREW
NP TITANIUM HEALING CAP [3MM]
NP TITANIUM HEALING CAP [5MM]
50 05 08
50 05 09
50 05 10
50 05 01
50 05 02
50 05 03
RP COVER SCREW
TITANIUM HEALING CAP RP [3MM]
TITANIUM HEALING CAP RP [5MM]
50 08 01 0.9 MM HEX LONG WRENCH ADAPTER
50 08 02 0.9 MM HEX WRENCH ADAPTER
Once the implant is placed, insert the cover screw or the titanium healing cap,
using the Hex adaptor [50 08 01/50 08 02].
WP COVER SCREW
WP TITANIUM HEALING CAP [3MM]
WP TITANIUM HEALING CAP [5MM]
NP KL IMPLANT Ø 3,3 X 08 MM
NP KL IMPLANT Ø 3,3 X 10 MM
NP KL IMPLANT Ø 3,3 X 12 MM
NP KL IMPLANT Ø 3,3 X 14 MM
RP KL IMPLANT Ø 3,7 X 06 MM
RP KL IMPLANT Ø 3,7 X 08 MM
RP KL IMPLANT Ø 3,7 X 10 MM
RP KL IMPLANT Ø 3,7 X 12 MM
RP KL IMPLANT Ø 3,7 X 14 MM
RP KL IMPLANT Ø 4,2 X 06 MM
RP KL IMPLANT Ø 4,2 X 08 MM
RP KL IMPLANT Ø 4,2 X 10 MM
RP KL IMPLANT Ø 4,2 X 12 MM
RP KL IMPLANT Ø 4,2 X 14 MM
WP KL IMPLANT Ø 4,7 X 08 MM
WP KL IMPLANT Ø 4,7 X 10 MM
WP KL IMPLANT Ø 4,7 X 12 MM
WP KL IMPLANT Ø 4,7 X 14 MM
10 02 01 T
10 02 01 LT
10 02 02 T
10 02 02 LT
10 02 03 T
10 02 03 LT
10 02 05 T
10 02 05 LT
1300
1500
1533 NT
LANCEOLATE DRILL [DS]
LONG LANCEOLATE DRILL [DS]
STARTUP DRILL Ø 2.35 MM [DS]
LONG STARTUP DRILL Ø 2.35 MM [DS]
PILOT DRILL Ø 2.8 MM [DS]
LONG PILOT DRILL Ø 2.8 MM [DS]
DRILL Ø 3.3 MM [DS]
LONG DRILL Ø3,3 MM [DS]
COUNTERSINK DRILL Ø 4.2 MM
COUNTERSINK DRILL Ø5.5 MM
STRAIGTH DRILL Ø 4.2 MM [DS]
S4 2133 L
S4 2137 L
S4 2142 L
S6 2148 L
10 06 05
7030
THREAD INITIATOR Ø 3.3 MM [YELLOW]
THREAD INITIATOR Ø 3.7 MM [RED]
THREAD INITIATOR Ø 4.2 MM [BLUE]
THREAD INITIATOR Ø 4.8 MM [GREEN]
PARALLELISER
GAUGE
51 33 08
51 33 10
51 33 12
51 33 14
51 37 06
51 37 08
51 37 10
51 37 12
51 37 14
51 42 06
51 42 08
51 42 10
51 42 12
51 42 14
51 47 08
51 47 10
51 47 12
51 47 14
NP KL IMPLANT 0.7 Ø 3,3 X 08 MM
NP KL IMPLANT 0.7 Ø 3,3 X 10 MM
NP KL IMPLANT 0.7 Ø 3,3 X 12 MM
NP KL IMPLANT 0.7 Ø 3,3 X 14 MM
RP KL IMPLANT 0.7 Ø 3,7 X 06 MM
RP KL IMPLANT 0.7 Ø 3,7 X 08 MM
RP KL IMPLANT 0.7 Ø 3,7 X 10 MM
RP KL IMPLANT 0.7 Ø 3,7 X 12 MM
RP KL IMPLANT 0.7 Ø 3,7 X 14 MM
RP KL IMPLANT 0.7 Ø 4,2 X 06 MM
RP KL IMPLANT 0.7 Ø 4,2 X 08 MM
RP KL IMPLANT 0.7 Ø 4,2 X 10 MM
RP KL IMPLANT 0.7 Ø 4,2 X 12 MM
RP KL IMPLANT 0.7 Ø 4,2 X 14 MM
WP KL IMPLANT 0.7 Ø 4,7 X 08 MM
WP KL IMPLANT 0.7 Ø 4,7 X 10 MM
WP KL IMPLANT 0.7 Ø 4,7 X 12 MM
WP KL IMPLANT 0.7 Ø 4,7 X 14 MM
JDTWKLF
JDTWKL
7040
7050 PK
7060 PK
JDTORQUE® RATCHET WRENCH
JDTORQUE® TORQUE WRENCH
C/A WRENCH
RATCHET WRENCH ADAPTER
LONG RATCHET WRENCH ADAPTER
50 05 01
50 05 02
50 05 03
50 05 05
50 05 06
50 05 07
50 05 08
50 05 09
50 05 10
RP COVER SCREW
TITANIUM HEALING CAP RP [3 MM]
TITANIUM HEALING CAP RP [5 MM]
NP COVER SCREW
NP TITANIUM HEALING CAP [3 MM]
NP TITANIUM HEALING CAP [5 MM]
WP COVER SCREW
WP TITANIUM HEALING CAP [3 MM]
WP TITANIUM HEALING CAP [5 MM]
50 08 01
50 08 02
50 08 04
50 08 05
50 08 06
0.9 MM HEX LONG WRENCH ADAPTER
0.9 MM HEX WRENCH ADAPTER
1.2 HEX LONG TORQUE WRENCH ADAPTER
1.2 MM HEX TORQUE WRENCH ADAPTER
1.2 MM HEX CONTRA-ANGLE WRENCH
FINISH DRILL
3.3 MM
10 02 03 T / 10 02 03 LT
3.7 MM
10 02 05 T / 10 02 05 LT
4.2 MM
10 02 05 T / 10 02 05 LT
4.7 MM
1533 N
* In D1 bone situations and accidents in areas near
anatomical or spaces Committed, you can use this
drill to confirm initiation deep socket.
0.7
All KLOCKNER® IMPLANT SYSTEM products comply with the laws and regulations applicable to medical devices, such as: European
directives MDD 93/42/ECC modified by 2007/47EC · Regulations of the United States FDA 21CFR 820 · Quality standards EN ISO 13485
and other applicable standards and regulations.
NP · RP · WP
WARNINGS
DON'T TIGHTEN [MAX 5 NCM] DURING THE INSERTION OF THE COVER SCREW OR THE TITANIUM HEALING CAP, IN ORDER
TO FACILITATE LATER REMOVAL.
50 33 08
50 33 10
50 33 12
50 33 14
50 37 06
50 37 08
50 37 10
50 37 12
50 37 14
50 42 06
50 42 08
50 42 10
50 42 12
50 42 14
50 47 08
50 47 10
50 47 12
50 47 14
IMPLANT
EPHITHELIAL PLACEMENT
50 05 05
50 05 06
50 05 07
reference listing
NP · RP · WP
NP · RP · WP
QUICK GUIDE
SOADCO S. L. is a manufacturer of surgical-medical material, specifically dental implants and related surgical-medical products. KLOCKNER of North America, inc is the official distributor in usa. SOADCO S. L., KLOCKNER of North America and/or
other official distributors do not practicemedicine or dentistry and therefore do not recommend either surgical techniques or dental-medical equipment for patients.
SOADCO S. L, KLOCKNER of North America, inc. and/or other official distributors do not guarantee a particular result or benefits arising from the use of such dental-medical equipment manufactured and/or sold by themselves, and decline / refuse
any responsibility regarding the use of the material based on the interpretation of the information described in this document, because a particular outcome cannot be guaranteed.
Any witness, opinion or instruction described in this document and distributed to any healthcare professional, clinician, researcher, or any qualified personnel are only their testimony, opinions, or instructions. these are not testimony, opinions, or
instructions from employees of SOADCO S. L. , KLOCKNER of North America, inc. and/or other official distributors.
Therefore, SOADCO S. L., KLOCKNER of North America, inc. and/or other official distributors are not responsible for any claim or statement made by such parties.
The products described in this document are for their acquisition and use only by dental-medical professionals appropriately trained and qualified in this field and must not be resold.
The devices described in this document are manufactured by:
SOADCO S. L, Avgda. Fiter i Rossell, 4 bis local nº 2 escaldes-engordany [Andorra] and distributed in usa by KLOCKNER of North America, inc. 175 sw 7 street, units 1103-1104 Miami fl - 33130 [usa]
The use and/or selection of an inappropriate treatment of any medical and/or surgical materials described in this document, is solely responsibility of the user of such material.
WARNING
NOT ALL KLOCKNER® IMPLANTS SYSTEM PRODUCTS ARE AVAILABLE IN EVERY COUNTRY
www.klocknerimplantsystem.com
0.7
NP · RP · WP
DIAMETER 3.3 MM
ALTERNATIVE TO Ø 0/2.35 MM
NP · RP · WP
QUICK GUIDE
WARNINGS
FAILURE TO FOLLOW THE RECOMMENDATIONS OF SURGICAL SEQUENCE CAN CAUSE:
- INTEGRATION DIFFICULTY OF THE IMPLANT, RESULTING IN OVERCOMPRESSION OF THE IMPLANT BED
- LACK OF PRIMARY STABILITY.
- OSSEOINTEGRATION FAILURE.
ALL INSTRUMENTS SHARPAND REVOLVING COMMITMENTS MAY INVADE ANATOMICALAREAS AS:
-NOSTRILS MAXILLARY SINES
-TOOTH NERVE.
-MENTAL FOREMAN
-LINGUALARTERY
SECURE THE INSTRUMENTS WITH A WIRE TO PREVENT THEM FROM BEING SWALLOWED OR ASPIRATED BY THE PATIENT.
ACCORDING TO MANUFACTURER'S INDICATIONS, EACH DRILL SHOULD NOT EXCEED 5 USES.
VERIFY THATALL DRILLS ARE IN GOOD CONDITION AND IN PERFECT CONDITIONS FOR USE.
ALWAYS FOLLOW THE DESCRIBED SEQUENCES, SINCE THE SIZE OF IMPLANTS IS CONNECTED WITH THE SIZE OF DRILLS.
BEFORE ITS USE, VERIFY THAT THE HAND PIECE STICKS THE DRILL PERFECTLY AND THAT THE SPIN IS RIGHT, CHECKING
INITIATOR · USE PROCEDURE
INITIATOR INSERTION
IMPLANT
S4 2133 L
S4 2137 L
THREAD INITIATOR Ø 3.3 MM [YELLOW]
S4 2142 L
ALLOW USE BY MANUAL FORM AND FOR
RATCHET OR TORQUE WRENCH
300 - 600 R.P.M.*
Ø 2.35 MM
DIAMETER 3.7 MM
PARALLELISER
300 - 600 R.P.M.
Ø 2.8 MM
PARALLELISER
1500 - 3000 R.P.M.
Ø 4.2 MM
GAUGE
20 R.P.M.
Ø 3.3 MM
IMPLANT
ALLOW USE BY MANUAL FORM AND FOR
RATCHET OR TORQUE WRENCH
THREAD INITIATOR Ø 4.8 MM [GREEN]
ALLOW USE BY MANUAL FORM AND FOR
RATCHET OR TORQUE WRENCH
ALLOW USE BY MANUAL FORM AND FOR
RATCHET OR TORQUE WRENCH
THREAD GUIDE STYLED
TYPE BONE
IMPLANT
IMPLANT INSERTION KL
DIAMETER IMPLANT
3.3
3.7
4.2**
D1
COMPLETE
D2
COMPLETE
D3
CORTICAL
D4
CORTICAL
Inserting the implant may be with a motor or ratchet or torque wrench, using the corresponding components.
STEP BY STEP
4.7**
D1
D2
D3
D4
BONE DENSITY CLASSIFICATION
AS MISCH
**4.2 / 4.7 MM IMPLANTS ARE NOT SUITED FOR BONE TYPE D1, D2.
300 - 600 R.P.M.*
Ø 2.35 MM
DIAMETER 4.2 MM
PARALLELISER
300 - 600 R.P.M.
Ø 2.8 MM
PARALLELISER
1500 - 3000 R.P.M.
Ø 4.2 MM
300 - 600 R.P.M.**
Ø 3.3 MM
GAUGE
20 R.P.M.
Ø 3.8 MM
IMPLANT WITH CARRIER
IMPLANT
ALTERNATIVE TO Ø 0/2.35 MM
1500 - 3000 R.P.M.
Ø 0/2.35 MM
IMPLANT
WARNINGS
DO NOT START THE OPERATION THREAD WITHOUT CHECKING THAT THE MANUAL FITS WITH THE INITIATOR IS CORRECT.
YOU SHOULD BE AWARE THAT THERE ARE RATCHET WRENCH TORQUE CONTROLAND MAY CREATE A FORCE THAT HURT
THE ONE CAUSING COMPRESSION APPARATUS AND MAY CAUSE EXCESSIVE ALVEOLAR TO THE BONE NECROSIS AND
RESULT IN LOSS OF POSTING.
IF THE RESISTANCE OF BONE PROGRESS IS LOW, WE ADVISED YOU TO NOT THREAD THE ENTIRE SOCKET BUT TO WORK
ON ½ O ¾ TOTAL DEPTHS.
* FOR MORE INFORMATION SEE TABLE THREAD PREPARATION GUIDE WITH INITIATOR.
RATCHET OR TORQUE WRENCH: IF THERE IS HIGH BONE RESISTANCE DURING INSERTION OF THE IMPLANT, THE
DIRECTION OF THE RATCHET OR TORQUE WRENCH SHOULD BE REVERSED, SCREWING THE IMPLANT COUNTERCLOCKWISE [OUT] FOR APPROXIMATELY TWO TURNS. THEN CHANGE THE
DIRECTION OF THE WRENCH AND CONTINUE THREADING CLOCKWISE [IN]. THIS RELEASES THE STRESS IN THE BONE
AND FACILITATES THREADING WORK. REPEAT THIS STEP AS MANY TIMES AS NECESSARY.
TO MAKE AN STRONG TORQUE FORCE IN THE INSIDE OF THE SURIGCAL ALVELOUS MAY CAUSE THE BONE TABLE TO
BREAK.
FAILURE TO FOLLOW THE RECOMMENDATIONS OF SURGICAL SEQUENCE CAN CAUSE DIFFICULTY IN PRIMER
INSERTION.
PLACEMENT WITH RATCHET OR TORQUE WRENCH
IN
300 - 600 R.P.M.*
Ø 2.35 MM
DIAMETER 4.7 MM
PARALLELISER
300 - 600 R.P.M.
Ø 2.8 MM
PARALLELISER
1500 - 3000 R.P.M.
Ø 4.2 MM
300 - 600 R.P.M.**
Ø 3.3 MM
GAUGE
20 R.P.M.
Ø 4.2 MM
IMPLANT WITH CARRIER
IMPLANT
ALTERNATIVE TO Ø 0/2.35 MM
1500 - 3000 R.P.M.
Ø 0/2.35 MM
JDTWKLF
JDTWKL
7050 PK
7060 PK
B-0042-EN
REV. 06
300 - 600 R.P.M.*
Ø 2.35 MM
PLACEMENT
WITH MOTOR
7040
C/A WRENCH
Position the hex drill in KL conveyor hex
connection.
It is important to verify that the adapter is
correctly positioned on the conveyor before
starting the screw maneuver.
Enter the implant at the implant site.
The working speed should be low [15-20 RPM],
and torque should not exceed 45 Ncm.
JDTORQUE® RATCHET WRENCH
JDTORQUE® TORQUE WRENCH
RATCHET WRENCH ADAPTER
LONG RATCHET WRENCH ADAPTER
INSERT
After removing the screw fastener ratchet or
torque adapter, position the initiator in the
adapter, and screw maneuver starts with the
ratchet wrench [IN] making slow rotational
movements.
IMPLANT
OUT
1500 - 3000 R.P.M.
Ø 0/2.35 MM
S6 2148 L
THREAD INITIATOR Ø 4.2 MM [BLUE]
THREAD INITIATOR Ø 3.7 MM [RED]
IMPLANT WITH CARRIER
ALTERNATIVE TO Ø 0/2.35 MM
1500 - 3000 R.P.M.
Ø 0/2.35 MM
THAT IRRIGATION IS ADEQUATE.
ECCENTRICIY OF ANY ROTARY CUTTING ITEM MAY CAUSE ALVEOLAR OVERSIZE.
FAILURE OF THE INSTRUMENT INSIDE THE MOUTH COULD LEAD TO ITS DETACHMENT IN THE ORAL CAVITY
WITH RISK OF SWALLOWING OR ASPIRATING.
IRRIGATION WITH PLENTY OF STERILE SOLUTION DURING THE DRILLING PROCESS IS ESSENTIAL TO
PREVENT POSSIBLE BONE TISSUE DAMAGE AND NO COMPROMISE THE IMPLANT OSSEOINTEGRATION.
LACK OF IRRIGATION WITH ROTARY INSTRUMENT USE MAY CAUSE BONE NECROSIS.
DO NOT EXCEED THE STATED SPEED.
ENGAGE LEVER FORCES DURING DRILLING, MAY CAUSE THE BREAK OF THE INSTRUMENT.
EXCEED 45 NCM TORQUE CAN DAMAGE THE SURGICAL MATERIAL CONNECTION IN CONTRA-ANGLE, AND
EVEN DAMAGE THE CONTRA-ANGLE HEAD.
PRESSURE SHOULD EXERCISE ALTERNATIVE ROUTING TECHNIQUE USING FLASH.
LOSS OF COLOR IDENTIFICATION OF DRILLS CAN CAUSE ERRORS IN THE STREAM OF DRILLING
KLOCKNER ® IMPLANT SYSTEM ASSUMES NO LIABILITY FOR DAMAGES RESULTING FROM BREACH OF THE
INSTRUCTIONS.
PARALLELISER
300 - 600 R.P.M.
Ø 2.8 MM
PARALLELISER
300 - 600 R.P.M.
Ø 3.3 MM
1500 - 3000 R.P.M.
Ø 5.5 MM
NOTE: IN THE FOLLOWING SEQUENCE SHOWN THE IMPLANT PLACEMENT OF 12 MM IN LENGTH.
300 - 600 R.P.M.**
Ø 4.2 MM
GAUGE
20 R.P.M.
Ø 4.7 MM
IMPLANT WITH CARRIER
IMPLANT
DESINTERTING
After reaching the desired depth with the
initiator, disconnect the adapter key, changing
the direction [OUT] to proceed with the
withdrawal.
Remove the drill from the transporter.
WARNINGS
VERIFY THAT THE CONTRA-ANGLE FIXED DRILL FITS CORRECTLY.
DO NOT START THE OPERATION THREAD WITHOUT CHECKING THAT THE RESERVE OF THE DRILL
WITH IMPLANT OR THREAD STARTER IS CORRECT.
OVERCOMING THE TORQUE OF 45 NCM MAY CAUSE DAMAGE TO THE CONTRA-ANGLE AND THE
DRILL
IF THE RESISTENCE THAT THE BONE OFFERES GOES OVER THE 45NCM, AND DOES NOT ALLOW
THE INSERATION OF THE IMPLANT ENTIRELY CONTINUE WITH THE WRENCH RATCHET.
FAILURE TO FOLLOW THE RECOMMENDATIONS OF SURGICAL SEQUENCE CAN CAUSE
DIFFICULTY IN IMPLANT INSERTION, RESULTING IN EXCESSIVE COMPRESSION IN THE IMPLANT
AREA. IMPLANT FORCED INTEGRATION CAN PRODUCE:
• DAMAGES IN CONNECTION.
• INSTRUMENTAL DAMAGE INDICATED FOR IMPLANT INSERTION.
• OSSEOINTEGRATION NON COMPRESSION EXCESSIVE IMPLANT IN BONE RECEIVER.