10,000 results
·
40ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
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