Home › Tekno-Medical Optik-Chirurgie GmbH › TEKNO®
TEKNO®
Tekno-Medical Optik-Chirurgie GmbH · Model 70110-22S · UDI-DI 04044684077367
10
510(k) clearances
11
Adverse events
1
Recalls
215
Facilities
Description
EXTRACT.FCPS.F.CHILDR.ENGL.PATT.FIG.22S
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2008-05-21 | Biomet Microfixation, Inc. | The Biomet Microfixation Obwegeser Ramus Clamp, Wide Right 01-7996 were incorrectly etched as the left part number 01-7997. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.