124 results · 23ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

Promogran Prisma™ Collagen Matrix with ORC and Silver

FDA 510(k)
FDA Unclassified ·Unknown

BISCOVER LED

FDA 510(k)
FDA Class 2 ·Dental

Ultrasound Transmission Gels

FDA 510(k)
FDA Class 2 ·Radiology

BIOSTINGER MENISCAL REPAIR DEVICE

FDA Adverse Event
Other ·LINVATEC CORP.·Product code HWC·August 27, 1999

SOFTFORM FACIAL IMPLANT

FDA Adverse Event
Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·February 28, 2000

SOFTFORM FACIAL IMPLANT

FDA Adverse Event
Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·December 15, 1999

CRANIOFIX TITANIUM CLAMP STERILE

FDA Adverse Event
Injury ·AESCULAP AG & CO. KG·Product code GXR·June 3, 1999

VASCO TIP BI 9/58

FDA Adverse Event
Malfunction ·VASCO MED·Product code DTB·June 16, 1999

SOFLEX THREE-PIECE FOLDABLE LENS

FDA Adverse Event
Injury ·CHIRON VISION CORP.·Product code HQL·April 30, 1999

GROSHONG 4 FR MIDLINE

FDA Adverse Event
Malfunction ·BARD ACCESS SYSTEMS·Product code DQO·March 1, 1999

B-D 10 ML SYRINGE LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO.·Product code FMI·March 1, 1999

VHS LAG SCREW

FDA Adverse Event
Injury ·BIOMET, INC.·Product code HRS·May 27, 1999

AUTO SUTURE MULTIFIRE GIA 80-4.8

FDA Adverse Event
Malfunction ·UNITED STATES SURGICAL CORP·Product code GAG·May 20, 1998

O.B. APPLICATOR TAMPON

FDA Adverse Event
Injury ·JOHNSON AND JOHNSON, S.A.·Product code HEB·March 29, 1999

UNK

FDA Adverse Event
Other ·SAFESKIN CORP.·Product code LYY·August 19, 1999

LP10 VOLUME VENTILATOR

FDA Adverse Event
Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·July 23, 1999

HAKIM PROGRAMMABLE VALVE WITH PRECHAMBER

FDA Adverse Event
Injury ·JOHNSON & JOHNSON PROFESSIONAL, INC. MEDOS S.A.·Product code JXG·January 21, 2000

RADIONICS

FDA Adverse Event
Injury ·RADIONICS, INC.·Product code JXG·March 8, 1999

SILTEX SALINE MAMMARY PROSTHESIS

FDA Adverse Event
Injury ·MENTOR·Product code FWM·May 11, 1999

SOFTFORM FACIAL IMPLANT

FDA Adverse Event
Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·September 27, 1999