FDA applicant

Kinetic Technology, Inc.

Pittsburgh, PA5 decisions1988–19921 recall

FDA records 5 decisions for Kinetic Technology, Inc. (Pittsburgh, PA) from 1988 to 1992: 5 510(k) clearances. All are in product code LXM (Manipulator, Plunger-Like Joint). 1 recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Kinetic 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 “Kinetic”

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

Kinetic Medical Products 63 Kinetic Concepts, Inc. 48 Kinetic Biomedical Services, Inc. 5 Kinetic Instruments, Inc. 2 Kinetic Surgical, LLC 2 Kinetic Rehabilitation Instruments, Inc. 1 Kinetic Resources, Inc. 1 Kinetic Innovative Seating System, LLC 1

Kinetic Technology, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Kinetic”