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

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ALPHA HISTOPLASMA ANTIGEN EIA MODEL HAG102

FDA 510(k)
FDA Class 2 ·Microbiology

Bur PM2-95 80K diam EC Ø4.5 St

FDA UDI
Bien-Air Surgery SA·17630055519884·

eTRAX™ Needle

FDA UDI
CIVCO MEDICAL INSTRUMENTS CO., INC.·00841436103213·Sterile needle, 14GA x 7cm with (7.6 tapered to...

LEKON

FDA UDI
C A I INDUSTRIES CORP·00807689004042·acupuncture needles

eTRAX™ Needle

FDA UDI
CIVCO MEDICAL INSTRUMENTS CO., INC.·10841436103227·Sterile needle, 14GA x 7cm with (7.6 tapered to...

GUTTA PERCHA POINTS

FDA UDI
DiaDent Group International·08806383556057·Gutta Percha Points is used to root canal filin...

GUTTA PERCHA POINTS

FDA UDI
DiaDent Group International·08806383500838·Gutta Percha Points is used to root canal filin...

Admiral

FDA UDI
Seaspine Orthopedics Corporation·10889981277208·Modular Trial, 14 x 13 x 7mm, 7 Deg Lordosis

The Orthodontic Store

FDA UDI
Young Innovations, Inc.·00843471156100·V D-Form 018

LATEX POWDER-FREE EXAMINATION GLOVES BLUE, POLYMER COATED, CONTAINS 50 MICROGRAMS OR LESS OF TOTAL WATER EXTRACTABLE PRO

FDA 510(k)
FDA Class 1 ·General Hospital

SURGITRON IEC II

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

Young Specialties

FDA UDI
Young Innovations, Inc.·00840326425862·NiTi SE Archwire, D-FORM .018 10EA

Ascendant

FDA UDI
Choice Spine, LP·10885862260482·

ARTIS ZEE III CEILING

FDA Adverse Event
Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·May 17, 2024

ARTIS ZEE III CEILING

FDA Adverse Event
Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·December 3, 2024

ARTIS Q ZEEGO

FDA Adverse Event
Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·September 29, 2025

ARTIS ZEE III CEILING

FDA Adverse Event
Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·April 29, 2026

ARTIS ZEE III CEILING

FDA Adverse Event
Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·April 1, 2026

ARTIS ZEEGO III (CHINA)

FDA Adverse Event
Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·December 26, 2023

ALTRX +4 NEUT 36IDX54OD

FDA Adverse Event
Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code LPH·May 9, 2013