43 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HEMI IMPLANT; MINI HEMI IMPLANT
FDA 510(k)
FDA Class 2
·Orthopedic
N/A
FDA UDI
GEORGE TIEMANN & CO.·B58211024010·
EVOTECH™
FDA UDI
ADVANCED STERILIZATION PRODUCTS SERVICES INC.·10705037000364·Channel connector tube, clear
ILIZAROV SYSTEMS
FDA UDI
MEDICALPLASTIC SRL·28033201841895·THREADED ROD SLOTTED 60MM LENGTH
GUTTA PERCHA POINTS
FDA UDI
DiaDent Group International·08806383502207·Gutta Percha Points is used to root canal filin...
L1 MANDIBLE
FDA UDI
KLS-Martin L.P.·00888118142191·BASE, PLATE, FRACTURE
NIAGARA® Lateral Access System
FDA UDI
VB Spine LLC·10888857517233·Posterior Blade, Size 80 mm
CIDEX OPA SOLUTION (0.55% ORTHRO-PHTHALALDEHYDE SOLUTION)
FDA 510(k)
FDA Class 2
·General Hospital
SWERV MAGNETOSTRICTIVE ULTRASONIC SCALER SYSTEM
FDA 510(k)
FDA Class 2
·Dental
STINGRAY LP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQY·March 26, 2025
SIDE STYLE HEMI ONE ARM WALKER 10240-1
FDA Adverse Event
Injury
·DRIVE MEDICAL·Product code ITJ·October 5, 2017
STINGRAY? LP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQY·May 29, 2026
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·May 9, 2013
PLV-102
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code CBK·August 27, 2014
9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 20, 2011
MICRUSFRAME10 5MM X 17CM
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code KRD·December 15, 2022
GALAXY G3 XSFT 4MM X 10CM
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code KRD·December 15, 2022
GALAXY G3 XSFT 4MM X 10CM
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code KRD·December 15, 2022
GALAXY G3 XSFT 3MM X 6CM
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code KRD·December 15, 2022
GALAXY G3 XSFT 2.5MM X 3.5CM
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code KRD·December 15, 2022