FDA applicant

Katalyst Surgical, LLC

Chesterfield, MO7 decisions2012–20220 recalls

FDA records 7 decisions for Katalyst Surgical, LLC (Chesterfield, MO) from 2012 to 2022: 7 510(k) clearances. Most are in product codes HQF (Laser, Ophthalmic) and GEI (Electrosurgical, Cutting & Coagulation &…). Its devices cite 12 predicates, 2 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 Katalyst Surgical, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2012high 2 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Katalyst Surgical, LLC by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Katalyst Surgical, LLC’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 “Katalyst”

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

Katalyst, Inc. 3

Katalyst Surgical, LLC

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Katalyst”