Data / Medical devices / Switzerland / Zurimed Technologies AG
Zurimed Technologies AG: FDA-registered device maker in Zurich, Switzerland, 2 510(k) clearances
Zurimed Technologies AG is registered with the FDA (registration 3034932459) in Zurich, Switzerland. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated January 2, 2026. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3034932459
- Address
- Lengghalde 5, Zurich, Switzerland, 8008
- Owner or operator
- ZuriMED Technologies AG (10092442)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- January 8, 2025
- Registered through
- 2027
- Brand names listed
- FiberLocker Implant, FiberLocker Instrument, FiberLocker PowerUnit, FiberLocker PowerUnit Charging Station, FiberLocker PowerUnit Handpiece, FiberLocker PowerUnit Motor Pack, FiberLocker PowerUnit Transfer Shield, FiberLocker System and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment | KIJ | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Mesh, Surgical, Non-Absorbable, Orthopaedics, Reinforcement Of Tendon | OWX | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
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 |
|---|---|---|---|---|---|---|
| January 2, 2026 | K253867 | FiberLocker Implant ; FiberLocker Instrument ; FiberLocker PowerUnit | OWX | Substantially Equivalent | ZuriMED Technologies AG | accessdata.fda.gov |
| December 11, 2024 | K241219 | FiberLocker System: FiberLocker Implant (SpeedPatch PET), FiberLocker Instrument (FiberLocker Instrument SN) | OWX | Substantially Equivalent | ZuriMED Technologies AG | accessdata.fda.gov |
Compare with other makers
- All makers of Mesh, Surgical, Non-Absorbable, Orthopaedics, Reinforcement Of Tendon
- All makers of Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment
Updated January 2, 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.