FDA applicant

Living Technology, Inc.

Warminster, PA4 decisions1989–19890 recalls

FDA records 4 decisions for Living Technology, Inc. (Warminster, PA) in 1989: 4 510(k) clearances. 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 Living Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Living Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Living Technology, 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 “Living”

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

Living Data Technologies Corporation 2

Living Technology, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Living”