FDA applicant

Electro Fiberoptics Corp.

Northborough, MA3 decisions1993–19940 recalls

FDA records 3 decisions for Electro Fiberoptics Corp. (Northborough, MA) from 1993 to 1994: 3 510(k) clearances. Most are in product codes HRX (Arthroscope) and EQH (Source, Carrier, Fiberoptic Light). 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, orthopedic panel, where it files most

How often FDA has decided Electro Fiberoptics Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Electro Fiberoptics Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Electro Fiberoptics Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Electro”

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

Electro-Nucleonics Laboratories, Inc. 41 Electro-Catheter Corp. 35 Electro-Biology, Inc. 28 Electro Medical Systems SA 11 Electro-Nucleonics, Inc. 9 Electro Therapeutic Devices, Inc. 8 Electro Med Supply, Inc. 8 Electro-Med Health Industries, Inc. 6 Electro-Diagnostic Instruments 4 Electro Medical Systems (Ems Sa) 3 Electro-Cap Intl., Inc. 3 Electro-Diagnostic Imaging, Inc. 2

Electro Fiberoptics Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Electro”