510(k) Report

FDA applicant

Point of View Optical Outlet, Inc.

Aventura, FL1 decision1995–19950 recalls

FDA records 1 decision for Point of View Optical Outlet, Inc. (Aventura, FL) in 1995: 1 510(k) clearance. All are in product code HQZ (Frame, Spectacle). 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 Point of View Optical Outlet, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Point of View Optical Outlet, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Point of View Optical Outlet, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Point”

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