Medical Device Manufacturer · US , San Diego , CA

Mast Biosurgery - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2008
2
Total
2
Cleared
0
Denied

Mast Biosurgery has 2 FDA 510(k) cleared medical devices. Based in San Diego, US.

Last cleared in 2021. Active since 2008. Primary specialty: General & Plastic Surgery.

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

510(k) submissions have been managed by QSR Consulting as regulatory consultant.

FDA 510(k) Regulatory Record - Mast Biosurgery

2 devices
1-2 of 2
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