FDA applicant

Technitex, Inc.

Houston, TX3 decisions1988–19890 recalls

FDA records 3 decisions for Technitex, Inc. (Houston, TX) from 1988 to 1989: 3 510(k) clearances. Most are in product codes HLR (Keratoscope, Battery-Powered) and HJA (Photokeratoscope). 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 Technitex, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Technitex, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Technitex, Inc.

Which product codes does it file in?

What has FDA decided for it lately?