FDA applicant

Reliant Laser Corp.

Foster City, CA3 decisions1992–19950 recalls

FDA records 3 decisions for Reliant Laser Corp. (Foster City, CA) from 1992 to 1995: 3 510(k) clearances. All are in product code GEX (Powered Laser Surgical Instrument). 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 Reliant Laser Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Reliant Laser Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Reliant Laser 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 “Reliant”

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

Reliant Technologies, Inc. 19

Reliant Laser Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Reliant”