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Ambler Surgical
AMBLER SURGICAL CORP. · Model Masket capsulorhexis forceps · UDI-DI 00190660063429
HNR
Prescription
10
510(k) clearances
888
Adverse events
16
Recalls
281
Facilities
Description
Masket capsulorhexis forceps, 4'', vaulted 11.0mm shanks, very delicate triangular grasping tips, guide pin, round handle
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.
