FDA applicant

Phantom Technologies, Inc.

Palo Alto, CA2 decisions1997–19980 recalls

FDA records 2 decisions for Phantom Technologies, Inc. (Palo Alto, CA) from 1997 to 1998: 2 510(k) clearances. All are in product code GEX (Powered Laser Surgical Instrument). Its devices cite 22 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Phantom Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Phantom 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 “Phantom”

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

The Phantom Laboratory, Inc. 4

Phantom Technologies, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Phantom”