1,272 results · 24ms · Sources: EU EUDAMED, US FDA

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BeneVision N12, BeneVision N15, BeneVision N17, BeneVision N19, BeneVision N22, BeneVision N1

FDA 510(k)
FDA Class 2 ·Cardiovascular

CoRoent

FDA UDI
Nuvasive, Inc.·00887517628510·CoRoent Ant TLIF Ti, 10x12x40mm 15°

Accufit

FDA UDI
Ortho Organizers, Inc.·00190707184216·Accufit Molar Bands Lower Left Second Molar 40 1/2

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112748·BARRON VACUUM PUNCH 7.25MM

Ophthalmic Knife

FDA UDI
KATENA PRODUCTS, INC.·00841668113424·CRESCENT KNIFE BEVEL UP (BX/5)

Ophthalmic Knife

FDA UDI
KATENA PRODUCTS, INC.·00841668113431·CRESCENT KNIFE DOUBLE BEVEL (BX/5)

MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·October 22, 2024

SPINAL EPIDURAL NEEDLES

FDA 510(k)
FDA Class 2 ·Anesthesiology

MODIFICATION TO PROMAX-XP, TENS AND MICROCURRENT DEVICE; PROMAX-TENS, TENS DEVICE; PROMAX-LIBRA, TENS DEVICE; PROMAX-MIC

FDA 510(k)
FDA Class 2 ·Neurology

ILET BIONIC PANCREAS

FDA Adverse Event
Injury ·BETA BIONICS·Product code QFG·June 6, 2024

BASE UNIT SERVO-U

FDA Adverse Event
Injury ·MAQUET CRITICAL CARE AB·Product code CBK·June 13, 2024

BASE UNIT SERVO-U

FDA Adverse Event
Injury ·MAQUET CRITICAL CARE AB·Product code CBK·June 13, 2024

AUTOSOFT XC

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·July 6, 2024

AUTOSOFT XC

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·July 6, 2024

AUTOSOFT XC

FDA Adverse Event
Injury ·UNOMEDICAL A/S·Product code FPA·July 6, 2024

AUTOSOFT XC

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·July 3, 2024

AUTOSOFT XC

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·July 3, 2024

AUTOSOFT XC

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·July 3, 2024

AUTOSOFT XC

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·July 3, 2024

CAREEVENT

FDA Adverse Event
Death ·PHILIPS MEDICAL SYSTEMS·Product code MSX·June 6, 2024