FDA applicant

Kinetic Instruments, Inc.

Bethel, CT2 decisions2001–20020 recalls

FDA records 2 decisions for Kinetic Instruments, Inc. (Bethel, CT) from 2001 to 2002: 2 510(k) clearances. All are in product code EBZ (Activator, Ultraviolet, For Polymerization). 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, dental panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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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 Technology, Inc. 5 Kinetic Biomedical Services, Inc. 5 Kinetic Surgical, LLC 2 Kinetic Rehabilitation Instruments, Inc. 1 Kinetic Resources, Inc. 1 Kinetic Innovative Seating System, LLC 1

Kinetic Instruments, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Kinetic”