FDA applicant

Medical Technique Instruments, Inc.

Redmond, WA2 decisions1989–19900 recalls

FDA records 2 decisions for Medical Technique Instruments, Inc. (Redmond, WA) from 1989 to 1990: 2 510(k) clearances. Most are in product codes HMW (Drape, Microscope, Ophthalmic) and IXA (Cassette, Radiographic Film). 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 Medical Technique Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Technique Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medical Technique Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?