25 results · 24ms · Sources: EU EUDAMED, US FDA

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SYNERGY HA COATED POROUS FEMORAL STEMS

FDA 510(k)
FDA Class 2 ·Orthopedic

Henry Schein

FDA UDI
HENRY SCHEIN, INC.·00304040062609·Endoflex Reamers 25 mm

TRUBYTE DENTURE CLEANSER/POLISHING COMPOUND

FDA 510(k)
FDA Class 1 ·Dental

TAMPAX SATIN TAMPONS, CLOSED END FLUSHABLE APPLICATOR; TAMPAX TAMPONS, OPEN END FLUSHABLE APPLICATOR

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

ULTRACISION HARMONIC SCALPEL HAND PIECE

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 13, 2006

ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54, 55

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

ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

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

ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

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

ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54, 55

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

ULTRACISION HARMONIC SCALPEL HAND PIECE

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54, 55

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code LFL·June 7, 2006

ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

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

ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

ULTRACISION HARMONIC SCALPEL HAND PIECE

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 13, 2006

ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code LFL·June 16, 2006

COULTER® LH 750 HEMATOLOGY ANALYZER

FDA Adverse Event
Malfunction ·BECKMAN COULTER·Product code GKZ·March 13, 2013

RESOLUTION HEMOSTASIS CLIPPING DEVICE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code MND·February 28, 2011

ACCU-CHEK SPIRIT

FDA Adverse Event
Injury ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·February 20, 2008

GMK-PRIMARY TIBIAL INSERT PS FIXED SIZE 3/10MM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 2, 2021