FDA applicant

Primed Instruments, Inc.

M9c 4h3, CA1 decision1993–19930 recalls

FDA records 1 decision for Primed Instruments, Inc. (M9c 4h3, CA) in 1993: 1 510(k) clearance. All are in product code FCL (Forceps, Biopsy, Non-Electric). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Primed 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 “Primed”

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

Primed Medical Products, Inc. 10 Primed Halberstadt Medizintechnik GmbH 1 Primed Products, Inc. 1 Primed, Inc. 1

Primed Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Primed”