55 results · 21ms · Sources: EU EUDAMED, US FDA

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IBA PROTON THERAPY SYSTEM, MODEL PROTEUS 235

FDA 510(k)
FDA Class 2 ·Radiology

Oticon

FDA UDI
Oticon A/S·05707131167460·ACTO, ITC P L BE

Osstell SmartPeg Type 101

FDA UDI
Osstell AB·09010522002131·ISQ Measurement Peg

DEBAKEY AORTIC CLAMP

FDA UDI
SONTEC INSTRUMENTS, INC.·B09921007660·DEBAKEY AORTIC CLAMP CUP-SHAPED JAW ANGLED LEFT

WHITE TOE NAIL SCISSORS

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896049703·WHITE TOE NAIL SCISSORS

DEBAKEY AORTIC CLAMP

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896003323·DEBAKEY AORTIC CLAMP CUP-SHAPED JAW ANGLED LEFT

Ear Tip PM008 Pack/100 pcs. (Grason)

FDA UDI
PATH medical GmbH·04260223142079·PATH MEDICAL is not manufacturer or Labeler of ...

Disposable Accessories Kit

FDA UDI
RESTORATION ROBOTICS, INC.·00850470007081·

UA Impression Sleeve

FDA UDI
BICON, LLC·00813110027023·UA6 SP-TP Impression Sleeves (3)

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·November 18, 2015

SYNTHES (USA) LARGE FRAGMENT LOCKING COMPRESSION PLATE (LCP) SYSTEM-T PLATE

FDA 510(k)
FDA Class 2 ·Orthopedic

TRI-FIX SPINAL FIXATION SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code HWC·August 3, 2015

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code HWC·August 4, 2015

INFINION 16

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 17, 2018

PLATE, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code HRS·October 8, 2015

MEGA SUTURECUT NEEDLE DRIVER INSTRUMENT

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·May 8, 2013

ALLEGRETTO WAVE EYE-Q

FDA Adverse Event
Injury ·WAVELIGHT GMBH·Product code LZS·September 12, 2014

LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

FDA Adverse Event
Injury ·ALLERGAN·Product code LTI·May 19, 2011

VA LOCKSCR Ø2.4 SELF-TAP L24 TAN

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·December 9, 2013