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

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Sonopet iQ Ultrasonic Aspirator System

FDA 510(k)
FDA Unclassified ·Unknown

ATLANTIS® Anterior Cervical Plate System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994235725·PLATE 6190070 ANTERIOR CERVICAL 70MM

ATLANTIS® Anterior Cervical Plate System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00763000867966·PLATE 6190070 ANTERIOR CERVICAL 70MM

Jawz Endomyocardial Biopsy Forceps

FDA UDI
ARGON MEDICAL DEVICES, INC.·00886333206797·Jaw Endomyocardial Biopsy Forceps 6F x 105cm St...

APEX Knee System

FDA UDI
Omni Life Science, Inc.·00841690196457·AK3 Congruent Tibial Insert Trials Size 1 - 5 Pan

Mariner Cortical

FDA UDI
Seaspine Orthopedics Corporation·10889987169491·CORTICAL SHANK, Cannulated, 9.0 X 70

Mariner Cortical

FDA UDI
Seaspine Orthopedics Corporation·10889981169497·CORTICAL SHANK, Cannulated, 9.0 X 70

APEX Knee System

FDA UDI
Omni Life Science, Inc.·00841690195160·AK3 Congruent Tibial Insert Trials Size 1 - 5 P...

Coral

FDA UDI
Seaspine Orthopedics Corporation·10889981029098·Prebent Rod 5.5 x 70

NA

FDA UDI
STRYKER CORPORATION·04546540996695·3.1mm x 19.1mm Straight Router

INVUITY BRITEFIELD MCCULLOCH RETRACTOR SYSTEM

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

UNIPLATE ANTERIOR CERVICAL PLATE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

PLUS SL

FDA Adverse Event
Injury ·SMITH & NEPHEW ORTHOPEDICS AG·Product code KWY·October 7, 2008

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 18, 2013

LUMAX 300 HF-T

FDA Adverse Event
Malfunction ·BIOTRONIK, SE & CO KG·Product code MRM·June 29, 2011

QUATTRO LINK ANCHOR 4.5MM

FDA Adverse Event
Malfunction ·CAYENNE MEDICAL·Product code MBI·April 20, 2023

HANDPIECE, EMAX 2 PLUS (ANSPACH DRILL), ROHS COMPLIANT

FDA Adverse Event
Injury ·BLUE BELT TECHNOLOGIES·Product code HBE·April 23, 2020

HANDPIECE, EMAX 2 PLUS (ANSPACH DRILL), ROHS COMPLIANT

FDA Adverse Event
Injury ·BLUE BELT TECHNOLOGIES·Product code HBE·April 24, 2020

BIOLOX DELTA OPTION CERAMIC HEAD 36MM

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code LZO·March 15, 2024

G7 LONGEVITY NEUTRAL 36MM E

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 14, 2024