Dgh Technology, Inc. is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dgh Technology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Scanmate Flex, MODEL DGH 6000 SCANMATE A, DGH 55 HANDHELD PACHYMETER (PACHMATE)
7
Total
7
Cleared
0
Denied
Dgh Technology, Inc. has 7 FDA 510(k) cleared medical devices. Based in Frazer, US.
Historical record: 7 cleared submissions from 1987 to 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Dgh Technology, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Entela, Inc., Underwriters Laboratories, Inc. and Regulatory Technology Services, LLC.
FDA 510(k) Regulatory Record - Dgh Technology, Inc.
7 devices
Cleared
Jul 31, 2017
Scanmate Flex
Radiology
89d
Cleared
Apr 05, 2010
MODEL DGH 6000 SCANMATE A
Radiology
158d
Cleared
Nov 07, 2003
DGH 55 HANDHELD PACHYMETER (PACHMATE)
Radiology
15d
Cleared
Mar 17, 1997
DGH MODEL 9000
Ophthalmic
84d
Cleared
Nov 02, 1992
DGH-500 PACHYMETER
Radiology
249d
Cleared
Jan 31, 1992
DGH-4000 A-SCAN/PACHYMETER
Radiology
204d
Cleared
Dec 04, 1987
DGH-3000A A-SCAN
Radiology
149d