FDA applicant
H & P Industries, Inc.
FDA records 5 decisions for H & P Industries, Inc. (Franklin, WI) from 1983 to 1990: 5 510(k) clearances. Most are in product codes GEC (Brush, Scrub, Operating-Room) and KMJ (Lubricant, Patient). 2 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided H & P Industries, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for H & P Industries, Inc. since 2007.
Recalls per year
1in 2011
2007high 1 (2010) · low 0 (2007)2026
Class I Class II/III not classified
Planning a device like H & P Industries, 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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