C&E GP Specialist, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
C&E GP Specialist, Inc. - FDA 510(k) Cleared Devices
Recent clearances: iSee (roflufocon D, roflufocon E) Daily Wear Orthokeratology Contact Lenses
1
Total
1
Cleared
0
Denied
C&E GP Specialist, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by C&E GP Specialist, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Eyereg Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - C&E GP Specialist, Inc.
1 devices