Data / Medical devices / France / Newclip Technics SAS
Newclip Technics SAS: FDA-registered device maker in HAUTE GOULAINE Loire-Atlantique, France, 34 510(k) clearances
Newclip Technics SAS is registered with the FDA (registration 3007143290) in HAUTE GOULAINE Loire-Atlantique, France. It lists 25 device types. The FDA files 34 510(k) clearances under its listings, the newest dated September 28, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007143290
- Address
- Pa De La Lande Saint Martin, HAUTE GOULAINE Loire-Atlantique, France, 44115
- Owner or operator
- NEWCLIP TECHNICS SAS (9089479)
- Roles
- Manufacturer, Specification developer
- First device listed
- September 27, 2006
- Registered through
- 2026
- Brand names listed
- ACTIV Ankle Prehensive plier, ACTIV Ankle Removal kit, ACTIV Ankle bending iron, ACTIV Ankle countersink, ACTIV Ankle drilling guide for plates, ACTIV Ankle forceps, ACTIV Ankle guide gauge, ACTIV Ankle instrumentation set and more
Devices it lists
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| September 28, 2026 | K262649 | Alians Forearm | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| July 28, 2026 | K261511 | Xpert Ankle | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| July 8, 2026 | K261191 | Alians Elbow S | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| May 29, 2026 | K261038 | Xpert PFP | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| March 11, 2026 | K253906 | Xpert Hand | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| October 1, 2025 | K250767 | Newclip Patient-matched instrumentation non sterile PSI | PBF | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| April 23, 2025 | K250155 | Xpert Knee | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| February 13, 2025 | K243912 | Newclip Patient-matched instrumentation non sterile PSI | PBF | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| November 7, 2024 | K240415 | Newclip Patient-matched instrumentation non sterile PSI | PBF | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| July 30, 2024 | K241539 | Activmotion S | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| October 25, 2023 | K221615 | Newclip Patient-matched instrumentation non sterile PSI | PBF | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| July 1, 2022 | K221395 | Footmotion Plating System | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| December 16, 2021 | K202803 | Activmotion S DTO | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| November 24, 2021 | K213214 | Xpert Wrist | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| November 17, 2020 | K202307 | Activ Fuse | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| February 27, 2018 | K173746 | Activmotion Range | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| January 16, 2018 | K173641 | Activ Ankle | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| January 4, 2018 | K171372 | Alians Elbow Locking Plating System | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| October 2, 2017 | K172596 | Large Screws Range | HWC | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| September 8, 2017 | K171510 | Footmotion Plating System | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| June 16, 2017 | K170843 | Alians Fragment Specific | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| April 24, 2017 | K170012 | Foot and Hand Motion | HWC | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| March 30, 2017 | K170310 | Alians Clavicle range | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| October 31, 2016 | K161448 | Footmotion Plating System | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| August 17, 2016 | K152289 | Alians Elbow Locking Plating System | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| June 3, 2016 | K160617 | Large Screws Range | HWC | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| January 30, 2015 | K141548 | HIGH TIBIAL OSTEOTOMY SYSTEM | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| January 26, 2015 | K143061 | Activ Ankle Locking Plating System | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| December 23, 2014 | K142502 | ALIANS ULNA LOCKING PLATING SYSTEM | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| June 19, 2013 | K130774 | UNIVERSAL DISTAL RADIUS SYSTEM | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| October 22, 2010 | K100944 | CLAVICLE LOCKING PLATE SYSTEM | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| December 16, 2009 | K091118 | FOOT AND HAND MOTION SYSTEM | HWC | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| December 22, 2006 | K063095 | HUMERUS LOCKING PLATING SYSTEM | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
| August 28, 2006 | K061917 | DISTAL RADIUS LOCKING PLATING SYSTEM | HRS | Substantially Equivalent | Newclip Technics | accessdata.fda.gov |
Compare with other makers
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- All makers of Screw, Fixation, Bone
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- All makers of Pliers, Surgical
- All makers of Guide, Surgical, Instrument
- All makers of Bit, Drill
Updated September 28, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.