Company · US

Vivorte, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2013 to 2015. Name variants (Inc, Corp, punctuation) are merged.

4510(k) clearances (0 in 12 months)

1recalls (0 in 12 months)

1recalls that name a 510(k)

Product codes

Code	Device	Records
MBP	Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)	3
MQV	Filler, Bone Void, Calcium Compound	2

Decided	510(k)	Device and applicant	Code
Jan 14, 2015	K143549	Vivorte Trabexus Vivorte, Inc.	MQV
Jan 14, 2015	K143547	Vivorte Trabexus EB Vivorte, Inc.	MBP
Sep 12, 2013	K130703	VIVORTE BVF Vivorte, Inc.	MBP
Aug 12, 2013	K131133	VIVORTE BVF LITE Vivorte, Inc.	MQV

Date	Firm and product	Code	Linked 510(k)
Jul 7, 2021	Vivorte, Inc. Vivorte Trabexus EB 10 cc Bone Void Filler -Fill bone and/or defect in skeletal system Model Number: 130703-10 Terminated	MBP	K130703 K143547