510(k) Report

FDA applicant

Progressive Affiliated Labs, Inc.

Mchenry, IL1 decision1976–19760 recalls

FDA records 1 decision for Progressive Affiliated Labs, Inc. (Mchenry, IL) in 1976: 1 510(k) clearance. All are in product code HPX (Lens, Contact (Polymethylmethacrylate)). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

How often FDA has decided Progressive Affiliated Labs, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Progressive Affiliated Labs, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Progressive Affiliated Labs, 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 “Progressive”

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