The Emerging Technologies Group is one of 10945 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Emerging Technologies Group - FDA 510(k) Cleared Devices
Recent clearances: KIS-III NON-SUBMERGED IMPLANT, SCREWS AND CYLINDERS, MT1A, MT1
7
Total
7
Cleared
0
Denied
The Emerging Technologies Group has 7 FDA 510(k) cleared medical devices. Based in North Palm Beach, US.
Historical record: 7 cleared submissions from 1996 to 1997. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by The Emerging Technologies Group Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by AllOnRx, LLC, as regulatory consultant.
FDA 510(k) Regulatory Record - The Emerging Technologies Group
7 devices
Cleared
Sep 09, 1997
KIS-III NON-SUBMERGED IMPLANT, SCREWS AND CYLINDERS
Dental
539d
Cleared
Sep 25, 1996
MT1A
Dental
190d
Cleared
Sep 25, 1996
MT1
Dental
190d
Cleared
Sep 25, 1996
MT-2
Dental
190d
Cleared
Sep 25, 1996
MT-3A
Dental
190d
Cleared
Sep 25, 1996
MT-2A
Dental
190d
Cleared
Sep 25, 1996
MT-X
Dental
190d