510(k) Report

FDA applicant

Fiber Imaging Technologies, Inc.

Newton, MA5 decisions1999–19990 recalls

FDA records 5 decisions for Fiber Imaging Technologies, Inc. (Newton, MA) in 1999: 5 510(k) clearances. Most are in product codes FCW (Light Source, Fiberoptic, Routine) and GCJ (Laparoscope, General & Plastic Surgery). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, gastroenterology and urology panel, where it files most

How often FDA has decided Fiber Imaging Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fiber Imaging Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Fiber Imaging Technologies, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Fiber Imaging Technologies, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Fiber”

FDA records each applicant name separately; these may or may not be the same firm.