17 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Bonecam Suture Anchor
FDA 510(k)
FDA Class 2
·Orthopedic
ECHO BI-METRIC MICROPLASTY HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304697904·
Orthos
FDA UDI
ORMCO CORPORATION·00889989030389·ORTHOS CM NITI ARCH16X22LOSM PK10
STRYKER BIPOLAR FORCEPS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
TVC IMAGING SYSTEM MODEL NIRS-MC7-70
FDA 510(k)
FDA Class 2
·Cardiovascular
IN TOUCH ZX
FDA Adverse Event
Malfunction
·STRYKER MEDICAL QUEBEC LP·Product code FNL·October 6, 2008
CAPITAL CONVECTIVE PATIENT
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code DWJ·June 27, 2013
PENTA 60-CM LENGTH PADDLE LEAD
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 21, 2011
OMNIFIX®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FMF·March 6, 2026
Quanta System Sterile Optical Laser Fiber, single use
FDA Enforcement
Class II
·Terminated·Quanta System, S.p.A.·June 16, 2021
BELIFU
FDA Adverse Event
Injury
·HONG QIANGXING (SHEN ZHEN) ELECTRONICS LIMITED·Product code GZJ·February 10, 2020
G7 PPS LTD ACET SHELL 50D
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PBI·April 9, 2020
CER BIOLOXD OPTION HD 36MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·June 14, 2019
G7 NEUTRAL E1 LINER 36MM D
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PBI·April 8, 2020
G7 PPS LTD ACET SHELL 50D
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PBI·April 8, 2020
CER BIOLOXD OPTION HD 36MM
FDA Adverse Event
Injury
·.·Product code LPH·April 8, 2020
MINIMED 770G OUS SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·June 18, 2025