FDA applicant

Burton Parsons & Co., Inc.

Mchenry, IL1 decision1976–19760 recalls

FDA records 1 decision for Burton Parsons & Co., 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 Burton Parsons & Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Burton Parsons & Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Burton Parsons & Co., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Burton Parsons & Co., Inc.’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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Other applicant names beginning “Burton”

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

Burton Medical Products Corp. 15 Burton 1

Burton Parsons & Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Burton”