510(k) Report

FDA applicant

Techna Vision

Santee, CA4 decisions1985–19860 recalls

FDA records 4 decisions for Techna Vision (Santee, CA) from 1985 to 1986: 4 510(k) clearances. Most are in product codes HRJ (Table, Instrument, Powered, Ophthalmic) and HPT (Perimeter, Automatic, Ac-Powered). 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 Techna Vision’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Techna Vision since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Techna”

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