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FCW TUBE STAND

FDA 510(k)
FDA Class 1 ·Radiology

Foot Compression Wrap Medium

FDA UDI
SUN SCIENTIFIC, INC.·00850051939237·Aero-Wrap™ Foot Compression Wrap is designed to...

Foot Compression Wrap Large

FDA UDI
SUN SCIENTIFIC, INC.·00856525007976·Aero-Wrap™ Foot Compression Wrap is designed to...

Foot Compression Wrap Small

FDA UDI
SUN SCIENTIFIC, INC.·00850051939220·Aero-Wrap™ Foot Compression Wrap is designed to...

HYLAMER NEUT 54OD X 28ID

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDL·July 21, 2011

FIBER OPTIC LIGHT CABLE

FDA Adverse Event
Injury ·KARL STORZ SE & CO. KG·Product code OAY·June 2, 2022

FIBER OPTIC LIGHT CABLE

FDA Adverse Event
Injury ·KARL STORZ SE & CO. KG·Product code OAY·June 7, 2022

FIBER OPTIC LIGHT CABLE, 230 CM, Ø3.5 MM

FDA Adverse Event
Malfunction ·KARL STORZ SE & CO. KG·Product code OAY·September 7, 2023

HIGH INTENSITY XENON LIGHT SOURCE

FDA Adverse Event
Malfunction ·KARL STORZ SE & CO. KG·Product code FCW·February 27, 2026

FIBER OPTIC LIGHT CABLE

FDA Adverse Event
Injury ·KARL STORZ SE & CO. KG·Product code OAY·June 15, 2023

Integra Surgical Luxtec MLX Light Source Catalog Numbers: 00MLX Product Usage: The Integra Luxtec MLX Light Source is designed to supply high intensity white light through a fiber optic cable for illumination of a surgical field during a surgical and or medical procedure.

FDA Recall
Terminated ·Integra LifeSciences Corp.·Product code FCW·October 14, 2011

Integra Surgical Luxtec MLX Light Source Catalog Numbers: 00MLXAU Product Usage: The Integra Luxtec MLX Light Source is designed to supply high intensity white light through a fiber optic cable for illumination of a surgical field during a surgical and or medical procedure.

FDA Recall
Terminated ·Integra LifeSciences Corp.·Product code FCW·October 14, 2011

Luxtec MLX 300 Watt Xenon Light Source, Model OOMLX; Surgical/Medical Light Source This light source is designed to supply high-intensity light to a fiber optic cable for illumination of a surgical field during a surgical and/or medical procedure.

FDA Recall
Terminated ·Integra LifeSciences Corp.·Product code FCW·March 7, 2011

Integra Surgical Luxtec MLX Light Source Catalog Numbers: 00MLXEU

FDA Recall
Terminated ·Integra LifeSciences Corp.·Product code FCW·October 14, 2011

SafeLight Fiber Optic Cable: Clear, 5MM X 10FT 3.05M, REF: 0233-050-100; Gray, 5MM X 10FT 3.05M, REF: 0233-050-200

FDA Recall
Open, Classified ·Stryker Corporation·Product code FCW·March 2, 2023

L9000 LIGHT SOURCE

FDA Adverse Event
Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code FCW·October 10, 2016

MLX 300W XENON LIGHTSOURCE

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

MLX 300W XENON LIGHTSOURCE

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

MLX 300W XENON LIGHTSOURCE

FDA Adverse Event
Malfunction ·INTEGRA BURLINGTON, MA, INC.·Product code FCW·July 1, 2015

UNKNOWN_ENDOSCOPY_PRODUCT

FDA Adverse Event
Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code FCW·September 9, 2015