Opusdent , Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Opusdent , Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Opusdent , Ltd. has 5 FDA 510(k) cleared medical devices. Based in Ra'Ananna, IL.
Historical record: 5 cleared submissions from 2000 to 2002. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Opusdent , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Opusdent , Ltd.
5 devices
Cleared
Aug 07, 2002
OPUSDUO EC DENTAL LASER SYSTEM
General & Plastic Surgery
90d
Cleared
Jan 08, 2002
OPUS SPECTRUM (A MODEL OF OPUS 20), MODEL 2ND
General & Plastic Surgery
26d
Cleared
Aug 30, 2001
OPUS 10 (WITH TOOTH WHITENING APPLICATION), MODEL 2ND
General & Plastic Surgery
84d
Cleared
Dec 12, 2000
OPUS 20, MODEL 1ST
General & Plastic Surgery
85d
Cleared
Jun 23, 2000
OPUS 10 DENTAL DIODE LASER
General & Plastic Surgery
87d