FDA applicant

Trophy Skin, Inc.

Frisco, TX3 decisions2014–20160 recalls

FDA records 3 decisions for Trophy Skin, Inc. (Frisco, TX) from 2014 to 2016: 3 510(k) clearances. Most are in product codes OAP (Laser, Comb, Hair) and NFO (Stimulator, Transcutaneous Electrical…). Its devices cite 4 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, physical medicine panel, where it files most

How often FDA has decided Trophy Skin, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2014high 1 (2014) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Trophy Skin, Inc. by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Trophy Skin, 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 “Trophy”

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

Trophy Radiologie 16 Trophy 15

Trophy Skin, 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 “Trophy”