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LINK Instruments - Fixation instruments
WALDEMAR LINK GmbH & Co. KG · Model 64-4159/98 · UDI-DI 04026575347698
HWD
Prescription
0
510(k) clearances
28
Adverse events
1
Recalls
91
Facilities
Description
Orthopaedic prosthesis instrument, reusable - General Instrument
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-03-10 | Biomet, Inc. | One lot of 30 mm screws was switched with one lot of 25 mm screws. |
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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.
