Preceptis Medical is one of 15045 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Preceptis Medical - FDA 510(k) Cleared Devices
Recent clearances: Hummingbird Tympanostomy Tube, HUMMINGBIRD(TM) TYMPANOSTOMY TUBE SYSTEM (TTS), PRECEPTIS TYMPANOSTOMY TUBE INSERTER
3
Total
3
Cleared
0
Denied
Preceptis Medical has 3 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Historical record: 3 cleared submissions from 2014 to 2015. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Preceptis Medical Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Preceptis Medical
3 devices