Medical Device Manufacturer · US , Mchenry , IL

Rexton, Inc. - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 1983

Recent clearances: REXTON MODEL 48 AND 49PP, PICCOLO K-AMP VC+, PICCOLO P-A1, PICCOLO P-AO AND PICCOLO ATC, LONG LIFE RX-12

21
Total
21
Cleared
0
Denied

Rexton, Inc. has 21 FDA 510(k) cleared ear, nose, throat devices. Based in Mchenry, US.

Historical record: 21 cleared submissions from 1983 to 1997.

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

FDA 510(k) Regulatory Record - Rexton, Inc.

21 devices
1-12 of 21
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