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

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CINtec Histology

FDA 510(k)
FDA Class 2 ·Pathology

NA

FDA UDI
Stryker Leibinger GmbH & Co. KG·04546540366696·PLATE BENDER, LEFT, 1.2/1.7MM

NA

FDA UDI
Stryker Leibinger GmbH & Co. KG·07613154731794·TENSION PLIERS FOR ANCHOR SCREWS

SILICONE SPHERES

FDA 510(k)
FDA Class 2 ·Ophthalmic

ULTRACISION HARMONIC SCALPEL BLADES WITH PROTECTIVE SLEEVE, MODELS DH105, DH145, SH105, SH145

FDA 510(k)
FDA Unclassified ·Unknown

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·August 6, 2025

ULTRACISION SURG DEV, BLADES 5MM, OPEN

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code LFL·June 15, 2006

ULTRACISION SURG DEV, BLADES 5MM, OPEN

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 19, 2006

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·October 29, 2014

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·August 15, 2011

HOMECHOICE PRO

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·July 8, 2013

PROSTHESIS, HIP, SEMI-CONSTRAINED, UNCEMENTED, METAL/POLYMER, POROUS

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code MBL·October 17, 2025

PROSTHESIS, HIP, SEMI-CONSTRAINED, UNCEMENTED, METAL/POLYMER, NON-POROUS, CALICU

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code MEH·October 15, 2025

MR Coils The MR Coil is intended to be used in conjunction with a Magnetic Resonance Scanner to produce diagnostic images of the anatomy of interest that can be interpreted by a trained physician.

FDA Enforcement
Class III ·Terminated·Invivo Corporation·October 28, 2020