FDA applicant

Simmler, Inc.

St. Louis, MO23 decisions1980–19890 recalls

FDA records 23 decisions for Simmler, Inc. (St. Louis, MO) from 1980 to 1989: 23 510(k) clearances. Most are in product codes KNK (Acid, Uric, Uricase (Colorimetric)) and CIX (Bromcresol Green Dye-Binding, Albumin). 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, clinical chemistry panel, where it files most

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

FDA decisions per year

No FDA decision for Simmler, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Simmler, 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 “Simmler”

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

Simmler & Son, Inc. 14

Simmler, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Simmler”