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Integra Container Lid, Size, Red; Container Lid, Size, Blue; Container Lid, Size, Red; Container Lid, Size, Gold; Container Lid, Size, Green; Container Lid, Full Size, Blue; Container Lid, Full Size, Red Catalogue Numbers: 730422, 730521, 730522, 730523, 730524, 730621, 730622 The Integra Sterilization Container is intended for use in hospitals and healthcare facilities to contain other medical devices that are to be steam sterilized (autoclaved) by the facility prior to use. Sterilized devices may be stored and transferred within the facility in the container per the healthcare facilities protocols. Integra provides these items to users as either as a tray and lid combination, just a tray, or just a lid.

FDA Recall
Terminated ·Integra York PA, Inc·Product code KCT·July 30, 2014

Miltex Premium Grade Self-Lock Chisel Blade Handle, Catalogue No. 4-405, manual surgical instrument.

FDA Recall
Terminated ·Integra York PA, Inc·Product code GDZ·March 11, 2016

Metzenbaum Scissors 7, Curved, Sterile The Metzenbaum Scissors 7, Curved Curved are single-use sterile surgical instruments intended for cutting and grasping tissue in general surgical procedures.

FDA Recall
Terminated ·Integra York PA, Inc·Product code LRW·October 28, 2016

Rochester-Pean Hemostatic Forceps 61/4, Curved, Sterile. The Rochester-Pean Hemostatic Forceps 61/4 Curved are single-use sterile surgical instruments intended for cutting and grasping tissue in general surgical procedures.

FDA Recall
Terminated ·Integra York PA, Inc·Product code GEN·October 28, 2016

UL PRO FUSED HEADLIGHT CABLE 9FT, 275CM

FDA Adverse Event
Malfunction ·INTEGRA YORK, PA INC.·Product code FST·November 22, 2016

ROTO-LOK ATRA ALLIS FCP 3.5X24

FDA Adverse Event
Injury ·INTEGRA YORK, PA INC.·Product code GCJ·November 23, 2016

MLX 300W XENON LIGHTSOURCE

FDA Adverse Event
Malfunction ·INTEGRA YORK, PA INC.·Product code FCW·November 22, 2016

PETIT-POINT O-HEGAR NH 5 SERR

FDA Adverse Event
Malfunction ·INTEGRA YORK, PA INC.·Product code FHQ·October 1, 2016

ULTRA-COAT MICRO EJECT KERRISON 40D UP 8 3MM

FDA Adverse Event
Malfunction ·INTEGRA YORK, PA INC.·Product code HAE·October 14, 2016

OSTEOTOME CP313-1 GUARDED 3.0MM BECKER

FDA Adverse Event
Malfunction ·INTEGRA YORK, PA INC.·Product code GFI·October 7, 2016

MLX 300W XENON LIGHTSOURCE

FDA Adverse Event
Malfunction ·INTEGRA YORK, PA INC.·Product code FCW·December 1, 2016

INTEGRATOR MALLET

FDA Adverse Event
Malfunction ·INTEGRA YORK, PA INC.·Product code LXM·October 7, 2016

VALVE 1375011 ESSAR REPLACEMENT

FDA Adverse Event
Malfunction ·INTEGRA YORK, PA INC.·Product code KCB·October 17, 2016

FERREIRA BREAST RETRACTOR W/FIBER OPTICS

FDA Adverse Event
Malfunction ·INTEGRA YORK, PA INC.·Product code GAD·September 15, 2015

FRAZIER SUCTION TUBE 8FR

FDA Adverse Event
Malfunction ·INTEGRA YORK, PA INC.·Product code EQH·September 16, 2015

MONOPOLAR CABLE 10 FEET

FDA Adverse Event
Malfunction ·INTEGRA YORK, PA INC.·Product code KNF·August 28, 2015

CARB-BITE STERNAL NH 7-3/4

FDA Adverse Event
Malfunction ·INTEGRA YORK, PA INC.·Product code GDF·July 16, 2015

FORCEPS MCEN27-2 PEDIATRIC BACKBITER

FDA Adverse Event
Malfunction ·INTEGRA YORK, PA INC.·Product code KAE·September 8, 2015

SCHEIN. AUTOCL U CONTRA A

FDA Adverse Event
Malfunction ·INTEGRA YORK, PA INC.·Product code EFB·August 6, 2015

RHOTON-TYPE HOOK 71/2 90D SSHP

FDA Adverse Event
Malfunction ·INTEGRA YORK, PA INC.·Product code GZX·September 8, 2015