41 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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VACUFLOW+ BLOOD COLLECTION SET, MODEL 52221/3/5; VACUFLOW+ WITH HOLDER BLOOD COLLECTION SET, MODEL 82021/3/5 WITH HOLDER
FDA 510(k)
FDA Class 2
·General Hospital
t:slim X2 Insulin Pump
FDA UDI
Tandem Diabetes Care, Inc.·00852162004798·t:slim X2 Insulin Pump, Reconditioned, 4YR Warr...
Preat
FDA UDI
Preat Corporation·00842092169506·Dynamic Zimmer TSV 5.7mm X 9mm Non-Engaging Tit...
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040179352·Diamond Discs
Zavation
FDA UDI
Zavation LLC·00842166122123·3-Level, 69mm Cervical Plate
CURE™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167700003690·
Spacelabs Healthcare
FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522118456·HOLTER LEADWIRES, EVO/ARIA, BROWN. 10PK
Spacelabs Healthcare
FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522126239·HOLTER LEADWIRES, EVO/ARIA, BROWN. 10PK
TUFF TT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·June 17, 2024
TUFF TT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·June 17, 2024
CURE™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167S1700003690·
BELLEGLASS HP OPACEOUS DENTIN
FDA 510(k)
FDA Class 2
·Dental
NUPRO PROPHYLAXIS PASTE WITH FLUORIDE AND TRICLOSAN
FDA 510(k)
FDA Class 1
·Dental
COOPERSURGICAL
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code ITX·May 29, 2026
TUFF TT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·July 1, 2024
TUFF TT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·July 9, 2024
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·October 5, 2015
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·March 12, 2013
RESTORE ULTRA
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·February 18, 2011
DIGOXIN REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC·Product code KXT·February 18, 2008