Ditron Precision, Ltd. is one of 489 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Ditron Precision, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Dental Implants and Abutments, MPI - MOLECULAR PRECISION IMPLANT, CPI - CYLINDRICAL PRECISION IMPLANT, OPI - ONE PIECE IMPLANT, DENTAL ABUTMENTS AND PR
2
Total
2
Cleared
0
Denied
Ditron Precision, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Netanya, IL.
Historical record: 2 cleared submissions from 2014 to 2016. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Ditron Precision, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Talmed , Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Ditron Precision, Ltd.
2 devices