18 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Stryker Self-Punching ICONIX
FDA 510(k)
FDA Class 2
·Orthopedic
High Density 144 Sublative iD (200 Pulse), 10-Pk
FDA UDI
SYNERON MEDICAL LTD·37290109951189·High Density 144 Sublative iD (200 Pulse), 10-Pk
MP Reconstruction Prosthesis
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575210718·Hip Prosthesis Stem,Size 002
MP Reconstruction Prosthesis
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575210749·Hip Prosthesis Stem,Size 005
MP Reconstruction Prosthesis
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575210732·Hip Prosthesis Stem,Size 004
MP Reconstruction Prosthesis
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575210701·Hip Prosthesis Stem,Size 001
MP Reconstruction Prosthesis
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575320677·Hip Prosthesis Stem,Size 00
MP Reconstruction Prosthesis
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575210756·Hip Prosthesis Stem,Size 006
MP Reconstruction Prosthesis
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575210725·Hip Prosthesis Stem,Size 003
ENDOSCOPIC MONOPOLAR INSTRUMENTS AND ACCESSORIES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DISPOSABLE INFUSION PUMP KIT, GO PUMP RAPID RECOVERY SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
GMK-SPHERE FEMORAL COMPONENT SPHERE CEMENTED SIZE 5 R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·September 2, 2020
GMK PRIMARY TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·May 26, 2025
TBD
FDA Adverse Event
Malfunction
·Product code KOD·April 5, 2018
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 17, 2013
CONTAK RENEWAL
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 23, 2011
PROLIEVE TEMPERATURE MONITOR
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·September 19, 2008
Exactech Equinoxe CAGE GLENOID, CEMENTED, beta curvature, Mates with: a) 47, 50, 53 head, Medium, Item Number 314-13-13, b) 47, 50, 53 head, Large, Item Number 314-13-14, c) 47, 50, 53 head, Extra Large, Item Number 314-13-15; Shoulder Arthroplasty
FDA Enforcement
Class II
·Ongoing·Exactech, Inc.·April 10, 2024