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Tecomet
TECOMET INC. · Model 00481700100 · UDI-DI 00841435123748
HTE
Prescription
0
510(k) clearances
137
Adverse events (1 deaths)
3
Recalls
175
Facilities
Description
SHARP HOOK 6"
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-09-24 | SpineFrontier, Inc. | Handles and heads may not be compatible. |
| 2013-09-24 | SpineFrontier, Inc. | Handles and heads may not be compatible. |
| 2013-09-24 | SpineFrontier, Inc. | Handles and heads may not be compatible. |
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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.