FDA applicant

John Branch

Irvine, CA1 decision1997–19970 recalls

FDA records 1 decision for John Branch (Irvine, CA) in 1997: 1 510(k) clearance. All are in product code LXQ (Cup, Eye). 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 John Branch’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for John Branch since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “John”

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

The John Bunn Co. 20 John O. Butler Co. 6 John F. Greer Co., Inc. 5 John Chatillon & Sons, Inc. 3 John Riccio 2 John J. Navar, M.D. 1 John Caunt Scientific, Ltd. 1 John W. King 1 John Wagner Associates, Inc. 1 John J Riccio 1 John M. Rayhack 1 John Mfg., Ltd. 1

John Branch

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “John”