Home › BLACK & BLACK SURGICAL, INC. › Black & Black Surgical
Black & Black Surgical
BLACK & BLACK SURGICAL, INC. · Model B61185X · UDI-DI 00840329831769
2
510(k) clearances
89
Adverse events
2
Recalls
76
Facilities
Description
TEBBETTS FIBEROPTIC RETRACTOR; 15CM X 20MM BLADE, WITHOUT TEETH, WITH ROUNDED EDGES
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2009-07-01 | Lumitex Inc | Adhesive which is used to attach LightMat to retractor may not have been tested to Medical standards. The vendor provided an adhesive strip that did not conform to Lumitex specifi |
| 2008-10-24 | Biomet Microfixation, Inc. | Fiber optic cable is missing from the Frederick's Converse Retractor Lot # 042408D08. |
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.
