86 results · 31ms · Sources: EU EUDAMED, US FDA

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Endo 6:1, T1 Line Endo 6 L, SIRONiTi Apex, T1 Spray

FDA 510(k)
FDA Class 1 ·Dental

Oticon

FDA UDI
Oticon A/S·05707131281203·H16V2, MINIBTE 312 WL 85 DBL

Ophthalmic Speculum

FDA UDI
KATENA PRODUCTS, INC.·00841668100189·MCINTYRE SPECULUM CLOSED WIRE

DeRoyal

FDA UDI
DEROYAL INDUSTRIES, INC.·00749756170246·THERA-BAND EXERCISE BAND

Ophthalmic Speculum

FDA UDI
KATENA PRODUCTS, INC.·00841668100158·KRATZ-BARRAQUER SPECULUM LARGE

Symmetry Surgical Ultra®

FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482055632·Ultra Instruments Clamp; Bulldog Vein Clamp; St...

HNM MEDICAL

FDA UDI
HNM STAINLESS, LLC.·00842962162071·BABY TISCHLER PUNCH, 8", 2MMX4MM BITE, W/LOCK

AUDIT MICROCV ASO LINEARITY SET, MODEL K721M-5

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

LC BRACKET ADHESIVE SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

HNM MEDICAL

FDA UDI
HNM STAINLESS, LLC.·00842962111161·BULLDOG VEIN CLAMP, 2", CVD, TITANIUM

BIOMET BONE CEMENT R 40X2

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·November 9, 2016

BIOMET BONE CEMENT V

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code MBB·December 1, 2016

BIOMET BONE CEMENT V

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code MBB·December 1, 2016

OPTIPAC-S 60 REFOBACIN BONE CEMENT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·June 14, 2016

REFOBACIN BONE CEMENT R 2X40G

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·February 2, 2018

OPTIPAC-S KNEE REFOBACIN PLUS BONE CEMNT

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·May 25, 2016

BIOMET BONE CEMENT 1X40G

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·July 22, 2016

BIOMET BONE CEMENT R 2X40G

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·July 9, 2016

OPTIPAC-S 60 REFOBACIN BONE CEMENT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·May 23, 2016

OPTIPAC-S 40 REFOBACIN PLUS BONE CEMENT

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·May 25, 2016