FDA applicant

Reliant Technologies, Inc.

Mountain View, CA19 decisions1994–20080 recalls

FDA records 19 decisions for Reliant Technologies, Inc. (Mountain View, CA) from 1994 to 2008: 19 510(k) clearances. Most are in product codes GEX (Powered Laser Surgical Instrument) and IMG (Stimulator, Ultrasound And Muscle, For Use In…). Its devices cite 60 predicates, 28 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 Reliant Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2008

2007high 6 (2007) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Reliant”

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

Reliant Laser Corp. 3

Reliant Technologies, 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?

Other applicant names beginning “Reliant”