Diamatrix
Diamatrix · Model F062 · UDI-DI 00813059014740
HNR
Prescription
10
510(k) clearances
888
Adverse events
16
Recalls
281
Facilities
Description
Gold Punctual Plug Forceps, Angled 5mm from bend to pointed blunt tips, Flat handle with hole pattern, 106mm total length, Stainless
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-03-25 | Katalyst Surgical, LLC | Field Safety Corrective Action for IFU in DEX Forceps and Scissors. |
| 2026-03-25 | Katalyst Surgical, LLC | Field Safety Corrective Action for IFU in DEX Forceps and Scissors. |
| 2026-03-25 | Katalyst Surgical, LLC | Field Safety Corrective Action for IFU in DEX Forceps and Scissors. |
| 2026-03-25 | Katalyst Surgical, LLC | Field Safety Corrective Action for IFU in DEX Forceps and Scissors. |
| 2026-03-25 | Katalyst Surgical, LLC | Field Safety Corrective Action for IFU in DEX Forceps and Scissors. |
| 2026-03-25 | Katalyst Surgical, LLC | Field Safety Corrective Action for IFU in DEX Forceps and Scissors. |
| 2026-03-25 | Katalyst Surgical, LLC | Field Safety Corrective Action for IFU in DEX Forceps and Scissors. |
| 2026-03-25 | Katalyst Surgical, LLC | Field Safety Corrective Action for IFU in DEX Forceps and Scissors. |
| 2026-03-25 | Katalyst Surgical, LLC | Field Safety Corrective Action for IFU in DEX Forceps and Scissors. |
| 2026-03-25 | Katalyst Surgical, LLC | Field Safety Corrective Action for IFU in DEX Forceps and Scissors. |
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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.
