392 results
·
30ms
·
Sources: EU EUDAMED, US FDA
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
FDA Pre-Market Approval
FDA Class 2
·AML(R) POROCOAT(R) ACETABULAR CUP PROSTHESIS
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
FDA Pre-Market Approval
FDA Class 2
·DURALOC(TM) 300S ACETABULAR CUP WITH POROCOAT(TM)
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
FDA Pre-Market Approval
FDA Class 2
·AML(R) POROCOAT(R) ACETABULAR CUP PROSTHESIS
Trimline
FDA UDI
ORMCO CORPORATION·00889989052299·LOWER RIGHT SECOND MOLAR TRIMLINE BAND SIZE 25
Arthrex®
FDA UDI
ARTHREX, INC.·00888867385603·Driver Shaft, T10, Non-retaining
DRIVER SHAFT, T10, NON-RETAINING
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·July 17, 2024
NEXGEN® TRABECULAR METAL™
FDA UDI
ZIMMER TRABECULAR METAL TECHNOLOGY INC.·00889024309982·
DRIVER SHAFT, T10, NON-RETAINING
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·August 8, 2023
DRIVER SHAFT, T10, NON-RETAINING
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·October 7, 2024
CHURCHILL 0.22 MICRON LIQUID FILTER SETS
FDA 510(k)
FDA Class 2
·General Hospital
DRIVER SHAFT, T10, NON-RETAINING
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·May 13, 2026
Boots Hearingcare 4
FDA UDI
Sonova AG·07613389793888·
Boots Hearingcare 2
FDA UDI
Sonova AG·07613389652536·
Boots Hearingcare 4
FDA UDI
Sonova AG·07613389793949·
Boots Hearingcare 4
FDA UDI
Sonova AG·07613389793918·
Boots Hearingcare 4
FDA UDI
Sonova AG·07613389793970·
Boots Hearingcare 2
FDA UDI
Sonova AG·07613389700671·
Boots Hearingcare 3
FDA UDI
Sonova AG·07613389700695·
Boots Hearingcare 2
FDA UDI
Sonova AG·07613389700657·
Boots Hearingcare 2
FDA UDI
Sonova AG·07613389652529·