FDA applicant

Palomar Medical Technologies, Inc.

Cary, NC24 decisions2000–20130 recalls

FDA records 24 decisions for Palomar Medical Technologies, Inc. (Cary, NC) from 2000 to 2013: 24 510(k) clearances. Most are in product codes GEX (Powered Laser Surgical Instrument) and ONG (Powered Laser Surgical Instrument With…). Its devices cite 67 predicates, 19 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 Palomar Medical Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2007high 2 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Palomar Medical 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 “Palomar”

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

Palomar Medical Products, Inc. 21 Palomar 2

Palomar Medical 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 “Palomar”