25 results · 20ms · Sources: EU EUDAMED, US FDA

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Ti 3Z Interbody System

FDA 510(k)
FDA Class 2 ·Orthopedic

OsteoMed

FDA UDI
OSTEOMED LLC·00845694016834·NeuroPack, 2 Medium Straight plate

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361010265·PedFuse Reset, SLD, 7.0mm x 70mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361010203·PedFuse Reset, SLD, 7.0mm x 40mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361010197·PedFuse Reset, SLD, 7.0mm x 35mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361010210·PedFuse Reset, SLD, 7.0mm x 45mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361010180·PedFuse Reset, SLD, 7.0mm x 30mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361010227·PedFuse Reset, SLD, 7.0mm x 50mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361010241·PedFuse Reset, SLD, 7.0mm x 60mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361010272·PedFuse Reset, SLD, 7.0mm x 75mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361010234·PedFuse Reset, SLD, 7.0mm x 55mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361010289·PedFuse Reset, SLD, 7.0mm x 80mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361010258·PedFuse Reset, SLD, 7.0mm x 65mm

RX DC X-RAY UNIT

FDA 510(k)
FDA Class 2 ·Dental

ATRIUM C-QUR OVT MESH

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

RD SET YI

FDA Adverse Event
Malfunction ·MASIMO - 52 DISCOVERY·Product code DQA·March 29, 2021

RD SET DCI

FDA Adverse Event
Malfunction ·MASIMO - 15750 ALTON PKWY·Product code DQA·February 10, 2023

SYNCHROMED II

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·June 20, 2013

UNKNOWN OPTEASE VENA CAVA FILTER

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code DTK·July 27, 2011

CARPENTIER-EDWARDS PERIMOUNT PLUS PERICARDIAL BIOPROSTHESIS

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code LWR·September 26, 2008