Home › Hayden Medical, Inc. › Hayden Medical
Hayden Medical
Hayden Medical, Inc. · Model 570-117 · UDI-DI 00840319752388
HXZ
Prescription
1
510(k) clearances
513
Adverse events
1
Recalls
247
Facilities
Description
Side Wire/Pin Cutter, Tungsten Carbide jaws, cuts up to .094" (2.4 mm) diameter hard wire, 9" (22.86 cm)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-11-20 | Zimmer Biomet, Inc. | Device has the potential for fracture during use. |
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.
