28 results · 20ms · Sources: EU EUDAMED, US FDA

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HUMAN IGG SUBCLASS KIT USE WITH THE BECKMAN IMAGE ANALYZER

FDA 510(k)
FDA Class 2 ·Immunology

NA

FDA UDI
DEPUY SPINE, LLC·10705034007137·SPINAL INSTRUMENT SPREADER INSERTER SHAFT

START VPS

FDA UDI
DANVILLE MATERIALS, LLC·00816594021266·START VPS,HEAVY,FLEX,ECON KIT

7mm washer 0.9mm Height

FDA UDI
Osteocentric Technologies, Inc.·00816950024856·7mm Washer 0.9mm Height

Tooth Tone

FDA UDI
ORTHO TECHNOLOGY, INC.·00190730014870·NiTi Coated Lower 014 10 archwires per pack

JOBST Custom Seamless Soft

FDA UDI
BSN-Jobst GmbH·04059993131174·CUSTOM SEAMLESS SOFT 1/AG-HT ONE LEG PANTY/CLOS...

JOBST Custom Seamless Soft

FDA UDI
BSN-Jobst GmbH·04059993129652·CUSTOM SEAMLESS SOFT 1/MID THIGH HIGH/CLOSED TO...

JOBST Custom Seamless Soft

FDA UDI
BSN-Jobst GmbH·04059993126170·CUSTOM SEAMLESS SOFT 1/CHAP STYLE/CLOSED TOE/SAND

JOBST Custom Seamless Soft

FDA UDI
BSN-Jobst GmbH·04059993130665·CUSTOM SEAMLESS SOFT 1/KNEE HIGH/CLOSED TOE/SAND

JOBST Custom Seamless Soft

FDA UDI
BSN-Jobst GmbH·04059993124114·CUSTOM SEAMLESS SOFT 1/PANTY/CLOSED TOE/SAND

JOBST Custom Seamless Soft

FDA UDI
BSN-Jobst GmbH·04059993132577·CUSTOM SEAMLESS SOFT 1/THIGH HIGH/CLOSED TOE/SAND

SYSTEM, BALLOON, INTRA-AORTIC AND CONTROL

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·January 29, 2026

WALLGRAFT TRACHEOBRONCHIAL ENDOPROSTHESIS AND UNISTEP DELIVERY SYSTEM

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

SYNTHETIC POWDER FREE (WHITE) VINYL PATIENT EXAMINATION GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

VCS-A SERIES CLAMP WITH DOPPLER ULTRASOUND, MODEL 09-0007-01 AND 09-0007-02

FDA 510(k)
FDA Class 2 ·Cardiovascular

VAPROX HC STERILANT

FDA Adverse Event
Malfunction ·STERIS CORPORATION·Product code MLR·June 12, 2025

ASR UNI FEMORAL IMPL SIZE 49

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·March 12, 2013

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·February 24, 2011

MICROSTAAR INJECTOR CARTRIDGE

FDA Adverse Event
Malfunction ·STAAR SURGICAL CO.·Product code KYB·February 21, 2008

TRAM 451N

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code DRT·March 14, 2007