24 results · 22ms · Sources: EU EUDAMED, US FDA

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Bovie J-Plasma Handpiece

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

CoRoent

FDA UDI
Nuvasive, Inc.·00887517637932·CoRoent Ant TLIF PEEK, 15x11x32mm 15°

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B167311513250·

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B167321513250·

WEBPAX, MODEL 200

FDA 510(k)
FDA Class 2 ·Radiology

STELLARIS PC VISION ENHANCEMENT SYSTEM

FDA 510(k)
FDA Class 2 ·Ophthalmic

2027971-2024-151325

FDA Adverse Event
Injury ·NOBEL BIOCARE USA, LLC·Product code DZE·December 2, 2024

EXPECT PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·May 19, 2026

EXPECT PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·September 24, 2025

STELLARIS VISION ENHANCEMENT SYSTEM

FDA Adverse Event
Injury ·BAUSCH + LOMB·Product code HQC·February 5, 2026

ACQUIRE? PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·October 10, 2025

EXPECT PULMONARY

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·November 14, 2024

EXPECT PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FCG·April 14, 2026

TENSION FREE VAGINAL TAPE

FDA Adverse Event
Injury ·ETHICON, INC.·Product code FTL·June 7, 2013

ASR ACETABULAR CUPS 50

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·June 30, 2011

SYNERGY

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·September 4, 2008

MENTOR MEMORYGEL BREAST IMPLANT

FDA Adverse Event
Injury ·MENTOR TEXAS·Product code FTR·March 13, 2024

MENTOR MEMORYGEL BREAST IMPLANT

FDA Adverse Event
Injury ·MENTOR TEXAS·Product code FTR·March 13, 2024

Precise Treatment Table. To be used as part of radiation therapy treatment process.

FDA Enforcement
Class II ·Terminated·Elekta, Inc.·April 17, 2013

All Elekta digital accelerators with electrons and beam modulator, MLCi/MLCi2, Agility or Asymmetric Heads Product Usage: Deliver of radiation to defined target volumes

FDA Enforcement
Class II ·Terminated·Elekta, Inc.·March 12, 2014