5,101 results · 30ms · Sources: EU EUDAMED, US FDA

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Ink, Arch Tracing

FDA classification
FDA Class 1 ·Ink, Arch Tracing

KEOS

FDA registration
KEOS·4 products·🇺🇸 United States

Kio Yamato Optics Inc.

FDA registration
Kio Yamato Optics Inc.·2 products·🇺🇸 United States

KAO CHEN ENTERPRISE CO., LTD.

FDA registration
KAO CHEN ENTERPRISE CO., LTD.·11 products·🇹🇼 Taiwan

KAO HOME ENT. CO., LTD.

FDA registration
KAO HOME ENT. CO., LTD.·1 product·🇹🇼 Taiwan

ACCUSIGN BZO, BIOSIGN BZO, STATUS BZO

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

ImmuTest Drugs of Abuse Screen Card

FDA UDI
AMEDITECH INC.·00816565020021·Benzodiazepine single drug dipcard

ACCUSIGN DOA3, DOA3(BZO/BAR/PCP), BZO/BAR/PCP, BIOSIGN DOA3, DOA3(BZO/BAR/PCP), BZO/BAR/PCP

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

Removal Tool, 3.5mm

FDA UDI
FLOWER ORTHOPEDICS CORPORATION·00840118118378·Orthopaedic implant reamer

AIMSCREEN BZO

FDA UDI
GERMAINE LABORATORIES, INC·00695684423254·Lateral flow immunoassay for the detection of B...

ACCUSIGN DOA2, DOA, BAR/BZO, BIOSIGN DOA2, BAR/BZO, STATUS DS BAR/BZO, SYVA RAPIDTEST D.A.U. 2 BAR/BZO

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

ACCUSIGN DOA 3/DOA 3 (BZO/BAR/PCP), BZO/BAR/PCP, BIOSIGN DOA 3/BZO/BAR/PCP, BIOSIGN BZO/BAR/PCP

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

KEOS LUMBAR IBFD

FDA Adverse Event
Injury ·KEOS·Product code MAX·February 20, 2019

Keos Lumbar Instrument

FDA UDI
KEOS·B0842003000310·

Keos Anterior Cervical Case/Caddy

FDA UDI
KEOS·B0842020201030·

Keos Anterior Cervical Case/Caddy

FDA UDI
KEOS·B0842020201220·

Lumbar IBFD

FDA UDI
KEOS·B084KTC22810120·

Keos Lumbar Case/Caddy

FDA UDI
KEOS·B0842000201030·

Keos Lumbar Instrument

FDA UDI
KEOS·B0842002000230·

Keos Lumbar Instrument

FDA UDI
KEOS·B0842004700030·