FDA applicant

Tekno-Medical

Tarzana, CA1 decision1991–19910 recalls

FDA records 1 decision for Tekno-Medical (Tarzana, CA) in 1991: 1 510(k) clearance. All are in product code DZL (Screw, Fixation, Intraosseous). 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, dental panel, where it files most

How often FDA has decided Tekno-Medical’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tekno-Medical since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Tekno-Medical”

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

Tekno Medical Optik-Chirurgie GmbH & Co. 2

Tekno-Medical

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Tekno-Medical”