Home › Device types › FFS
Image, Illumination, Fiberoptic, For Endoscope
FDA product code FFS · Class 2 · Gastroenterology, Urology
384
Registered devices
340
Adverse events
2
Recalls
26
510(k) clearances
Devices with this code
Surgical Direct — Surgical Direct, Inc.Surgical Direct — Surgical Direct, Inc.Surgical Direct — Surgical Direct, Inc.Surgical Direct — Surgical Direct, Inc.Surgical Direct — Surgical Direct, Inc.Surgical Direct — Surgical Direct, Inc.Surgical Direct — Surgical Direct, Inc.Surgical Direct — Surgical Direct, Inc.Surgical Direct — Surgical Direct, Inc.Surgical Direct — Surgical Direct, Inc.Surgical Direct — Surgical Direct, Inc.Surgical Direct — Surgical Direct, Inc.Fiber Optic Light Cable — GULF FIBEROPTICS, INC.Surgical Direct — Surgical Direct, Inc.Surgical Direct — Surgical Direct, Inc.Fiber Optic Light Cable — GULF FIBEROPTICS, INC.Surgical Direct — Surgical Direct, Inc.Surgical Direct — Surgical Direct, Inc.NA — Richard Wolf GmbHNA — Richard Wolf GmbHNA — Richard Wolf GmbHSurgical Direct — Surgical Direct, Inc.Surgical Direct — Surgical Direct, Inc.Fiber Optic Light Cable — GULF FIBEROPTICS, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-05-03 | Cook Inc. | Cook Inc. is initiating a voluntary recall of the Vue Optic Visualization Source and the Flexor Vue Deflecting Endoscopic System because it was determined that |
| 2007-04-09 | Smith & Nephew, Inc Endoscopy Division | Several units were manufactured using a power supply that contains a 1 amp fuse where a 5 amp fuse is required. When the unit's power supply draws more that 1A |
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