47 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
VOLUSON E6/E8/E8 EXPERT DIAGNOSTIC ULTRASOUND SYSTEM MODEL: H48681BD/ H48681BX/ H48681BM
FDA 510(k)
FDA Class 2
·Radiology
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526780842·LEVAMED ACTIVE ANKLE SUP SLVR R VI
Preat
FDA UDI
Preat Corporation·00842092108123·Preci Ball Increase Retention Tool
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587T1012360·10mm TLIF Implant 12mm Wide 36mm Length
Infiniti Plus™ Needle Guide
FDA UDI
CIVCO MEDICAL INSTRUMENTS CO., INC.·10841436102732·Sterile needle guide with (14 x 147cm) telescop...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587T10123670·10mm TLIF Implant 12mm Wide 36mm Length 7 Degrees
MODIFICATION TO IMPLANTABLE CLIP
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
RIZA BAND STRETCHER (RBS)-60000
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
AVANTAGE INLAY SIZE 50/28
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code LPH·December 15, 2016
TGS UKA SYSTEM
FDA Adverse Event
Injury
·ALEXANDRIA RESEARCH TECHNOLOGIES, INC·Product code HSX·March 22, 2013
TGS UKA KNEE SYSTEM
FDA Adverse Event
Injury
·ALEXANDRIA RESEARCH TECHNOLOGIES, INC.·Product code HSX·May 6, 2013
UNKNOWN BIOMET AVANTAGE INSERT
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LPH·February 16, 2017
AVANTAGE E1 INSERT DIA28 S56
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·July 21, 2016
UNKNOWN BIOMET AVANTAGE INSERT
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LPH·February 16, 2017
G7 BISPHERICAL SHELL 50D
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·December 15, 2025
CA090, DIRECT DRIVE LCA 3/BX
FDA Adverse Event
Malfunction
·APPLIED MEDICAL RESOURCES·Product code FZP·October 11, 2016
AVANTAGE INSERT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·June 2, 2017
TGS UKA SYSTEM
FDA Adverse Event
Injury
·CAYENNE MEDICAL, INC·Product code HSX·February 12, 2014
TGS UKA SYSTEM
FDA Adverse Event
Injury
·CAYENNE MEDICAL, INC.·Product code HSX·September 25, 2014
TGS UKA KNEE SYSTEM
FDA Adverse Event
Injury
·ALEXANDRIA RESEARCH TECHNOLOGIES, INC.·Product code HSX·September 10, 2013