Medical Device Manufacturer · US , San Antonio , TX

Artiberia - FDA 510(k) Cleared Devices

79 submissions · 79 cleared · Since 1985
79
Total
79
Cleared
0
Denied

Artiberia has 79 FDA 510(k) cleared medical devices. Based in San Antonio, US.

Historical record: 79 cleared submissions from 1985 to 1985. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Artiberia Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Artiberia
79 devices
1-12 of 79

Looking for a specific device from Artiberia? Search by device name or K-number.

Search all Artiberia devices
Filters