10,000 results
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123ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LAPORASCOPIC SURGICAL INSTRUMENTS /GENERAL USE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MANUAL SURGICAL INSTRUMENT FOR GENERAL USE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MANUAL SURGICAL INSTRUMENTS FOR GENERAL USE
FDA 510(k)MANUAL SURGICAL INSTRUMENT FOR GENERAL USE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
LAPAROSCOPIC SURGICAL INSTRUMENTS FOR GENERAL USE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MANUAL SURGICAL INSTRUMENT FOR GENERAL USE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MANUAL SURGICAL INSTRUMENTS FOR GENERAL USE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
FDA UDI
PARCUS MEDICAL LLC·00816342025072·Suture Pull Handle, Unsterile
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
FDA UDI
PARCUS MEDICAL LLC·00816342021531·Mallet
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code MDM·October 21, 2025
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
FDA Adverse Event
Malfunction
·SMITH & NEPHEW, INC.·Product code MDM·August 22, 2018
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code MDM·June 2, 2018
MANUAL SURGICAL INSTRUMENT FOR GENERAL USE
FDA Adverse Event
Injury
·OWENS & MINOR IHALYARD·Product code KDC·January 13, 2021
CURVED CANAL FINDERMANUAL SURGICAL INSTRUMENT FOR GENERAL USE
FDA Adverse Event
Malfunction
·SYMMETRY MEDICAL MANUFACTURING, INC·Product code HTR·April 11, 2023
MATTA IM CANAL FINDERMANUAL SURGICAL INSTRUMENT FOR GENERAL USE
FDA Adverse Event
Malfunction
·SYMMETRY MEDICAL MANUFACTURING INC·Product code HTR·April 11, 2023
ULTRACISION SURG DEV, BLADES 5MM, ENDO
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code LFL·September 15, 2006
ULTRACISION HARMONIC ACE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·March 21, 2014
ULTRACISION HARMONIC ACE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·March 21, 2014
NUVASIVE XLIF INSTRUMENTS
FDA Adverse Event
Malfunction
·NUVASIVE, INC.·Product code LXH·May 22, 2024
NUVASIVE XLIF INSTRUMENTS
FDA Adverse Event
Malfunction
·NUVASIVE, INC.·Product code LXH·April 17, 2023