26 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
neXus Ultrasonic Surgical Aspirator System
FDA 510(k)
FDA Unclassified
·Unknown
PIVOX™ Oblique Lateral Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169598928·TRIAL 2190160 O25 IB 27MM 0 DEG 8X60
ProEtch
FDA UDI
SILMET LTD·07290016787474·Dental Adhesive
OSE
FDA UDI
ORTHODONTIC SUPPLY & EQUIPMENT COMPANY INC·00810042122109·Stainless Steel Open Coil Spring - 3 x 12" - .0...
My Medical
FDA UDI
My Medical Store LLC·G4251901600·Joseph Hook 8mm
190-160
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668101087·HELVESTON "BARBIE" RETRACTOR
ZZOMA POSITIONAL SLEEPER MODEL 001
FDA 510(k)
FDA Class 2
·Dental
SUPRATHEL WOUND AND BURN DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
DUETTO MT
FDA Adverse Event
Malfunction
·QUANTA SYSTEM S.P.A.·Product code GEX·April 14, 2022
BIOLOX DELTA CER LNR 36MM E
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LZO·February 5, 2026
RINGLOC-X E1 H/W 56/36MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·April 27, 2026
BIOLOX DELTA CER LNR 40MM G
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·April 27, 2026
HEARTSTART FRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 18, 2013
CRYSTALENS
FDA Adverse Event
Injury
·EYEONICS, INC.·Product code HQL·February 9, 2007
PRIME PLUS (R) BARIATRIC MATTRESS
FDA Adverse Event
Malfunction
·PRIMUS MEDICAL LLC·Product code IKY·September 18, 2014
AVAN E1 INSERT 28 S 52
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·March 6, 2025
BIOLOX DELTA CER LNR 32MM E
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·September 8, 2025
RINGLOC BIPOLAR VIVACIT-E
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code LPH·September 10, 2025
MEDTRONIC DEEP BRAIN STIMULATION ELECTRODE
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code NHL·May 25, 2021
BIOLOX DELTA CER LNR 36MM E
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·November 13, 2025