77 results · 26ms · Sources: EU EUDAMED, US FDA

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Novapak Nasal Sinus Packing and Stent

FDA 510(k)
FDA Class 1 ·Ear, Nose, Throat

PILLING

FDA UDI
TELEFLEX INCORPORATED·24026704513929·

NA

FDA UDI
Synthes GmbH·10886982144348·3.0MM CANNULATED SCREW SHORT THREAD/23MM

36M - MSHA Miners

FDA UDI
Certified Safety Manufacturing, Inc.·00766588026206·36M - MSHA Miners

Diamond Orthopedic, LLC

FDA UDI
DIAMOND ORTHOPEDIC, LLC·B551DMD2026230·3.0mm, Cannulated Screw, Short Thd., 23mm

Medical Facets NC

FDA UDI
MEDICAL FACETS NC LLC·M933MDF2026230·3.0mm Cannulated Screw, Short Thread, 23mm

ABSORBENT PAPER POINTS

FDA UDI
DiaDent Group International·08806383513418·"An absorbent paper points is an endodontic pap...

5.0 MM DIAMETER POLYAXIAL SCREWS (MOSS MIAMI 6.35MM SYSTEM)

FDA 510(k)
FDA Class 2 ·Orthopedic

PURESPERM 40 AND PURESPERM 80

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

ABL90 FLEX PLUS ANALYZER

FDA Adverse Event
Malfunction ·RADIOMETER MEDICAL APS·Product code CHL·March 12, 2026

MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 27, 2026

ABL90 FLEX PLUS ANALYZER

FDA Adverse Event
Malfunction ·RADIOMETER MEDICAL APS·Product code CHL·March 12, 2026

PUMP 1886 780G OUS BLE PUMP MG/DL

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·January 27, 2026

I-STAT TROPONIN (HS-TNI ) CARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE INC.·Product code MMI·April 14, 2026

PUMP 1886 780G OUS BLE PUMP MG/DL

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·January 28, 2026

MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 27, 2026

MINIMED 780G OUS SYSTEM BLE CONNECT 3.0 MMOL/L

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·January 29, 2026

CAPTURE-R READY SCREEN

FDA Adverse Event
Malfunction ·IMMUCOR, INC.·Product code KSZ·October 21, 2008

V.A.C. THERAPY SYSTEM

FDA Adverse Event
Death ·KCI USA, INC.·Product code OMP·August 4, 2011

SYNCHROMED II

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·July 2, 2013