FDA applicant
Frank J. Biehl
FDA records 1 decision for Frank J. Biehl (San Jose, CA) in 1990: 1 510(k) clearance. All are in product code IRO (Vibrator, Therapeutic). 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 Frank J. Biehl’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Frank J. Biehl since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Frank J. Biehl’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) ReportOther applicant names beginning “Frank”
FDA records each applicant name separately; these may or may not be the same firm.