267 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·CHARITE ARTIFICIAL DISC
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·CHARITE ARTIFICIAL DISC
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·CHARITE ARTIFICIAL DISC
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·CHARITE ARTIFICIAL DISC
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·IN MOTION ARTIFICIAL DISC
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·IN MOTION LUMBAR ARTIFICIAL DISC
Paparella
FDA UDI
MEDTRONIC XOMED, INC.·00681490031073·VENT TUBE 1040006 10PK PAPA PR 1.14 SIL
Paparella
FDA UDI
MEDTRONIC XOMED, INC.·00763000039196·VENT TUBE 1040006 10PK PAPA PR 1.14 SIL
SMALL HUDSON POWER ADAPTER
FDA UDI
Osteocentric Technologies, Inc.·00810097803756·SMALL HUDSON POWER ADAPTER
25GA Illuminating Laser Probe. SMA 905
FDA UDI
Peregrine Surgical, Llc·00632307001710·25GA Illuminating Laser Probe. SMA 905
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481110382·LOCATOR Abutment R-Tx, Narrow CrossFit Internal...
Baby Gorilla/Gorilla Plating System
FDA UDI
Paragon 28, Inc.·00889795034427·Gorilla, Fibular, Straight, Hook, 06-Hole
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710820400060·Zadik Calcaneal Guide, 40mm x 6°
BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM-LINEZOLID-GRAM POSITIVE
FDA 510(k)
FDA Class 2
·Microbiology
SURE LOCK,A34,10 PK,BLUE LEVER,CURBELL
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828183352·SURE LOCK,A34,10 PK,BLUE LEVER,CURBELL
SURELOCK, CURBELL, BLUE, 14 PK
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828185943·SURELOCK, CURBELL, BLUE LEVER, 14 PACK
Device, Impotence, Mechanical/Hydraulic
FDA Pre-Market Approval
FDA Class 3
·TITAN INFLATABLE PENILE PROSTHESIS
Agent, Bulking, Injectable For Gastro-Urology Use
FDA Pre-Market Approval
FDA Class 3
·ENTERYX PROCEDURE KIT
BI MENTUM ALTRX LNR 53 28
FDA Adverse Event
Injury
·DEPUY IRELAND - 3015516266·Product code LZO·September 5, 2025
GYNECARE MORCELLEX* TISSUE MORCELLATOR
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code HET·April 8, 2013