ClearanceBrief
Company ยท US

Preceptis Medical

FDA 510(k) clearances and medical device recalls filed under this name, 2014 to 2022. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
ETDTube, Tympanostomy5

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jul 27, 2022K221254Hummingbird Tympanostomy Tube System
Preceptis Medical, Inc.
ETD
Jun 5, 2020K200952Hummingbird Tympanostomy Tube System
Preceptis Medical, Inc.
ETD
Sep 21, 2015K151830Hummingbird Tympanostomy Tube
Preceptis Medical
ETD
Apr 23, 2015K142282HUMMINGBIRD(TM) TYMPANOSTOMY TUBE SYSTEM (TTS)
Preceptis Medical
ETD
Aug 22, 2014K133921PRECEPTIS TYMPANOSTOMY TUBE INSERTER
Preceptis Medical
ETD

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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