Medical Device Manufacturer · US , Maineville , OH

Refractron Technologies Corp. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2009
1
Total
1
Cleared
0
Denied

Refractron Technologies Corp. has 1 FDA 510(k) cleared medical devices. Based in Maineville, US.

Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: Dental.

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

FDA 510(k) Regulatory Record - Refractron Technologies Corp.

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