FDA applicant
Biotech Medical Instruments Corp.
FDA records 1 decision for Biotech Medical Instruments Corp. (Marion, OH) in 1998: 1 510(k) clearance. All are in product code DZE (Implant, Endosseous, Root-Form). 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 Biotech Medical Instruments Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Biotech Medical Instruments Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Biotech Medical Instruments 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) ReportOther applicant names beginning “Biotech”
FDA records each applicant name separately; these may or may not be the same firm.