FDA applicant
Frantz Medical Development, Ltd.
FDA records 5 decisions for Frantz Medical Development, Ltd. (New York, NY) from 1987 to 1998: 5 510(k) clearances. Most are in product codes LZH (Pump, Infusion, Enteral) and DXR (Ballistocardiograph). 1 recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Frantz Medical Development, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Frantz Medical Development, Ltd. since 2007.
Recalls per year
1in 2007
Class I Class II/III not classified
Planning a device like Frantz Medical Development, Ltd.’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 “Frantz”
FDA records each applicant name separately; these may or may not be the same firm.