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Novo Surgical Inc.
NOVO SURGICAL, INC. · Model OP7126-57 · UDI-DI 00842331189784
HNR
Prescription
10
510(k) clearances
888
Adverse events
16
Recalls
280
Facilities
Description
thorpe conjunctival fixation forceps, 2x3 teeth, w/ platform, 3 3/4" (9.5 cm), 0.12 mm teeth
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.
