510(k) Report

FDA applicant

Medical Technical Products

Laguna Hills, CA8 decisions1987–19940 recalls

FDA records 8 decisions for Medical Technical Products (Laguna Hills, CA) from 1987 to 1994: 8 510(k) clearances. Most are in product codes HQC (Unit, Phacofragmentation) and FRN (Pump, Infusion). 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 Medical Technical Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Technical Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medical Technical Products’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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