Home › BR Surgical, LLC › BR Surgical, LLC
BR Surgical, LLC
BR Surgical, LLC · Model BR46-88203 · UDI-DI 00840183530488
KAE
Prescription
10
510(k) clearances
82
Adverse events
1
Recalls
224
Facilities
Description
Frontal Sinus Forceps, through cutting, with delicate flat jaws, shaft 90° upturned, width of cut 1.5mm, backward opening, 120mm working length, with cleaning port
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-01-31 | Aesculap Inc | The forceps have been used in ways not covered by the design resulting in breakage of the clamps. |
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.
