ClearanceBrief
Company ยท US

Aptis Medical, LLC

FDA 510(k) clearances and medical device recalls filed under this name, 2005 to 2019. 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
KXEProsthesis, Wrist, Hemi-, Ulnar5

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 3, 2019K190599Aptis Medical Distal Radio Ulnar Joint Implant
Aptis Medical, LLC
KXE
Apr 3, 2015K142569Aptis Medical Distal Radio Ulnar Joint Implant
Aptis Medical, LLC
KXE
Oct 24, 2008K082839DISTAL RADIO-ULNAR JOINT IMPLANT
Aptis Medical, LLC
KXE
Dec 7, 2005K053119DISTAL RADIO-ULNAR JOINT IMPLANT
Aptis Medical, LLC
KXE
Jan 26, 2005K040497DISTAL RADIO-ULNAR JOINT IMPLANT
Aptis Medical, LLC
KXE

Latest recalls

DateFirm and productCodeLinked 510(k)
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