Home › Device types › FDG
Retractor, Fiberoptic
FDA product code FDG · Class 1 · Gastroenterology, Urology
402
Registered devices
89
Adverse events
2
Recalls
2
510(k) clearances
Devices with this code
Spineart Surgical Illuminator — Lumitex, Inc.Thompson Surgical Instruments Large Lightmat 75mm — Lumitex, Inc.BR Surgical, LLC — BR Surgical, LLCSnowden-Pencer — STERIS CORPORATIONLife Spine Surgical Illuminator — Lumitex, Inc.Globus Medical 4mm ACMI Cable Adapter — Lumitex, Inc.St. Marks Hand Retractor — SONTEC INSTRUMENTS, INC.Novus N-Sight Disposable Surgical Light — Lumitex, Inc.N/A — BLACK & BLACK SURGICAL, INC.Fiber Optic Light Wand — FLEXBAR MACHINE CORPORATIONSpinal Elements Adapter - Olympus — Lumitex, Inc.Carnegie Surgical LLC — Carnegie Surgical LLCPhotonGuide XT System — INVUITY, INC.N/A — BLACK & BLACK SURGICAL, INC.RETRACTOR — KLS-Martin L.P.Spinal Elements PL Retractor Light — Lumitex, Inc.N/A — BLACK & BLACK SURGICAL, INC.Medacta Interntational Adapter - Wolf — Lumitex, Inc.Carnegie Surgical LLC — Carnegie Surgical LLCAlphatec Spine Storz Cable Adaptor — Lumitex, Inc.Snowden-Pencer — STERIS CORPORATIONInnerVision® — DIVERSATEK HEALTHCARE, INC.N/A — BLACK & BLACK SURGICAL, INC.Lumitex Surgical Light Cable — Lumitex, Inc.
Recent 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 confor |
| 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 docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
