FDA applicant

Active Optical Systems, Ltd./Efraim Bidas

Petach Tikva, IL1 decision2005–20050 recalls

FDA records 1 decision for Active Optical Systems, Ltd./Efraim Bidas (Petach Tikva, IL) in 2005: 1 510(k) clearance. All are in product code GEX (Powered Laser Surgical Instrument). Its devices cite 2 predicates, 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, general and plastic surgery panel, where it files most

How often FDA has decided Active Optical Systems, Ltd./Efraim Bidas’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Active Optical Systems, Ltd./Efraim Bidas since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Active Optical Systems, Ltd./Efraim Bidas by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Active”

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

Active Electronics, Inc. 7 Active Life Scientific, Inc. 3 Active Vertical Correctors, Inc. 2 Active Corp. 1 Active Optical Systems, Ltd. 1 Active Signal Technologies, Inc. 1 Active Protective Technologies, Inc. 1

Active Optical Systems, Ltd./Efraim Bidas

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Active”