41 results · 22ms · Sources: EU EUDAMED, US FDA

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Tigereye CTO-Crossing Catheter

FDA 510(k)
FDA Class 2 ·Cardiovascular

Accufit

FDA UDI
Ortho Organizers, Inc.·00190707183813·Accufit Molar Bands Lower Right First Molar 33

NA

FDA UDI
Stryker Leibinger GmbH & Co. KG·07613252634393·PED. MAND. DISTRACTOR, 2x2 LEFT, 30 MM

Life Instruments

FDA UDI
Life Instrument Corporation·M93072013300F0·Flat Cobb Elevator 30mm 7" handle

Life Instruments

FDA UDI
Life Instrument Corporation·M930720133000·Long Cobb Elevator 30mm 7" handle

Symmetry Olsen

FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00841785103728·

ABSORBENT PAPER POINTS

FDA UDI
DiaDent Group International·08806383511186·"An absorbent paper points is an endodontic pap...

Viceroy

FDA UDI
DIOMEDICAL CO.,LTD.·08800113905245·VICEROY Rod - 6.0 (D)6x(L)330mm

SOVEREIGN BIPOLAR INSTRUMENTS

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

MAGNETOM TRIO QUADRATURE TX/RX HEAD COIL

FDA 510(k)
FDA Class 2 ·Radiology

BECKER TEAR DROP

FDA UDI
The Wells Johnson Company·B458201330000·Cannula, Becker Tear Drop, specify length, diam...

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351101236·LAP- Electrode, monop., Ø5mm, l=330mm "J" - ...

BIPOLAR MACRO FORCEPS D:5/ 310MM

FDA Adverse Event
Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

ARCHITECT TACROLIMUS

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code MLM·January 28, 2013

BIPOLAR MARYLAND DISS.FCPS 5MM 310MM

FDA Adverse Event
Malfunction ·AESCULAP AG & CO KG·Product code GEI·March 9, 2015

JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

FDA Adverse Event
Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 29, 2014

JAW INS. BIP.MARYLAND DISS.FEN.5/310MM

FDA Adverse Event
Malfunction ·AESCULAP AG & CO. KG.·Product code GEI·January 13, 2015

DEXCOM G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM, DEXCOM SHARE SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code MDS·December 14, 2015

MARYLAND GSP.FORCEPS FEN.5/310MM HF CON.

FDA Adverse Event
Malfunction ·AESCULAP AG & CO. KG·Product code GEI·February 19, 2014

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·November 23, 2017