Medical Device Manufacturer · US , Waltham , MA

Astra Tech, Inc. - FDA 510(k) Cleared Devices

28 submissions · 28 cleared · Since 1994

Recent clearances: LOFRIC PRIMO, LOFRIC HYDRO-KIT, ATLANTIS IN ZIRCONIA FOR DENTSPLY ANKYLOS IMPLANT, ATLANTIS LATER ABUTMENT IN ZIRCONIA, ATLANTIS(TM) ABUTMENT AND ATLANTIS(TM) CROWN ABUTMENT FOR KEYSTONE GENESIS IMPLANT, ATLANTIS GEMINI(TM) ABUTMENT...

28
Total
28
Cleared
0
Denied

Astra Tech, Inc. has 28 FDA 510(k) cleared dental devices. Based in Waltham, US.

Historical record: 28 cleared submissions from 1994 to 2012.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Astra Tech, Inc.

28 devices
1-12 of 28
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