30 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INTERFUSE L INTERVERTEBRAL BODY FUSION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
PIVOX™ Oblique Lateral Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169605084·SPACER 2131540 OLIF25 27MM 6 DEG 16X40
NC Screw-retained Abutment
FDA UDI
BIO CONCEPT Co., Ltd.·06947600303381·
ArgenIS
FDA UDI
ARGEN CORPORATION, THE·D818131540·MUA SB RC 4.5GH Ang30
OsteoMed
FDA UDI
OSTEOMED LLC·00845694046183·PrimaLIF LLIF PEEK Implant, 15mm X 22mm X 40mm,...
Freedom Pedicle Screw System
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215027049·
CREATION
FDA UDI
Gc Orthodontics America Inc.·D78813154000101·CREATION ROTH 018/U4&5 -7T 0A
IH 15° Anatomic Abutment
FDA UDI
SURCAM - MEDICAL DEVICES AND DEVELOPMENTS LTD·07290120484382·
APEX ELECTRIC HANDPIECE SYSTEM
FDA 510(k)
FDA Class 1
·Dental
GRANITEC DUAL-CURE CORE BUILD-UP, N'DURANCE DIMER CORE
FDA 510(k)
FDA Class 2
·Dental
BIM400 IMPLANT MAGNET
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·December 19, 2017
COCHLEAR BAHA ATTACT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·June 26, 2016
ATTRACT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·October 15, 2015
COCHLEAR BAHA ATTACT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 17, 2016
BIM400 IMPLANT MAGNET
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 17, 2016
SP MAGNET 3
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·September 13, 2016
COCHLEAR BAHA ATTRACT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 14, 2016
BIM400 IMPLANT MAGNET
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·October 8, 2025
SURESCAN
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·October 1, 2014
SONOSURG SCISSORS 5MM O.D., HF SERIES
FDA Adverse Event
Malfunction
·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code LFL·May 15, 2013