FDA applicant

Electro-Biology, Inc.

Parsippany, NJ28 decisions1983–19993 recalls

FDA records 28 decisions for Electro-Biology, Inc. (Parsippany, NJ) from 1983 to 1999: 28 510(k) clearances. Most are in product codes KWQ (Appliance, Fixation, Spinal Intervertebral Body) and KTT (Appliance, Fixation, Nail/Blade/Plate…). Its devices cite 4 predicates, 3 of them its own earlier devices. 3 recalls are 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-Biology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Electro-Biology, Inc. since 2007.

Recalls per year

1in 2019

2007high 1 (2016) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Electro-Biology, 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 “Electro-Biology”

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 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 Fiberoptics Corp. 3 Electro-Cap Intl., Inc. 3 Electro-Diagnostic Imaging, Inc. 2

Electro-Biology, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Electro-Biology”