28 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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POWDERED VINAL EXAM GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040014233·Zirlux 16+ 0M1 98.5X22
MaXcess
FDA UDI
Nuvasive, Inc.·00887517065483·MaXcess Decomp Suction, 10FR Short
CoRoent
FDA UDI
Nuvasive, Inc.·00887517275820·CoRoent Large MP Trial, 14x9x23/28mm 4°
EZ2C
FDA UDI
FGX INTERNATIONAL INC.·00193033277027·
EZ2C
FDA UDI
FGX INTERNATIONAL INC.·00193033277041·
EZ2C
FDA UDI
FGX INTERNATIONAL INC.·00193033277010·
EZ2C
FDA UDI
FGX INTERNATIONAL INC.·00193033277034·
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0134140·Trial, TLIF, 27L OB STR 7Deg, 14mm
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0144140·Trial, TLIF, 32L OB STR 7Deg, 14mm
INSET I
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 4, 2025
KWIKKMODEL
FDA 510(k)
FDA Class 2
·Dental
R & D DESIGNATION AP-035
FDA 510(k)
FDA Class 2
·Dental
16CM MIN. INVASIVE ATTACHMENT
FDA Adverse Event
Malfunction
·THE ANSPACH EFFORT, INC.·Product code HBC·March 29, 2013
MINICAP TRANSFER SET
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·March 19, 2013
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·August 14, 2014
PINNACLE MTL INS NEUT36IDX52OD
FDA Adverse Event
Injury
·DEPUY INTL., LTD.·Product code KWA·March 4, 2011
EMAX 2 MOTOR
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBC·June 6, 2015
8CM ANGLE ATTACHMENT, BLACK, MAX
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBC·October 9, 2014
G7 VIT E NEUTRAL LNR 36MM F
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·November 14, 2022