FDA applicant

Fiberoptic Medical Products, Inc.

Philadelphia, PA5 decisions1988–19940 recalls

FDA records 5 decisions for Fiberoptic Medical Products, Inc. (Philadelphia, PA) from 1988 to 1994: 5 510(k) clearances. Most are in product codes CCW (Laryngoscope, Rigid) and EOQ (Bronchoscope (Flexible Or Rigid)). 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, anesthesiology panel, where it files most

How often FDA has decided Fiberoptic Medical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fiberoptic Medical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Other applicant names beginning “Fiberoptic”

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

Fiberoptic Sensor Technlogies, Inc. 11 Fiberoptic Fabrications, Inc. 1

Fiberoptic Medical Products, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Fiberoptic”