FDA applicant

Seiler Instrument & Mfg. Co., Inc.

St. Louis, MO1 decision1988–19880 recalls

FDA records 1 decision for Seiler Instrument & Mfg. Co., Inc. (St. Louis, MO) in 1988: 1 510(k) clearance. All are in product code HOH (Spectacle, Operating (Loupe), Ophthalmic). 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, ophthalmic panel, where it files most

How often FDA has decided Seiler Instrument & Mfg. Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Seiler Instrument & Mfg. Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Seiler Instrument & Mfg. Co., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Seiler Instrument & Mfg. Co., Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Seiler”

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

Seiler Precision Microscopes 1

Seiler Instrument & Mfg. Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Seiler”