FDA applicant
Allo Pro Corp.
FDA records 16 decisions for Allo Pro Corp. (Clearwater, FL) from 1981 to 1990: 16 510(k) clearances. Most are in product codes JDI (Prosthesis, Hip, Semi-Constrained…) and KWA (Prosthesis, Hip, Semi-Constrained (Metal…). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Allo Pro Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Allo Pro Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Allo Pro Corp.’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