ClearanceBrief
Company ยท US

Benvenue Medical, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2007 to 2020. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MAXIntervertebral Fusion Device With Bone Graft, Lumbar4
NDNCement, Bone, Vertebroplasty2
NKBThoracolumbosacral Pedicle Screw System1
OCJSpinal Channeling Instrument, Vertebroplasty1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 21, 2020K201427Trivergent Spinal Fixation System
Benvenue Medical, Inc.
NKB
Jul 2, 2020K193172Luna XD Ti Interbody Fusion System
Benvenue Medical, Inc.
MAX
May 23, 2019K183560Luna 3D GEN2 Interbody Fusion System
Benvenue Medical, Inc.
MAX
Nov 17, 2016K162431Luna 3D Interbody Fusion System
Benvenue Medical, Inc.
MAX
Nov 20, 2014K142023LUNA INTERBODY SYSTEM
Benvenue Medical, Inc.
MAX
Aug 14, 2014K141141KIVA VCF TREATMENT SYSTEM
Benvenue Medical, Inc.
NDN
Jan 24, 2014K132817KIVA VCF TREATMENT SYSTEM
Benvenue Medical, Inc.
NDN
Jul 10, 2007K070293BENVENUE VCF OSTEO COIL SYSTEM
Benvenue Medical, Inc.
OCJ

Latest recalls

DateFirm and productCodeLinked 510(k)
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