FDA applicant

Phase-R Corp.

New Durham, NH1 decision1987–19870 recalls

FDA records 1 decision for Phase-R Corp. (New Durham, NH) in 1987: 1 510(k) clearance. 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 Phase-R Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Phase-R Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Phase-R Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Phase-R Corp.’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 “Phase-R”

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

Phase Medical, Inc. 1 Phase Medical Systems, Inc. 1 Phase One Medical 1 Phase One Disign Co. 1 Phase I Corp. 1 Phase Change 1

Phase-R Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Phase-R”