142 results · 23ms · Sources: EU EUDAMED, US FDA

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Hyper GP (tisilfocon A) Daily Wear Contact Lens

FDA 510(k)
FDA Class 2 ·Ophthalmic

CoRoent

FDA UDI
Nuvasive, Inc.·00887517567574·CoRoent Ant TLIF PEEK, 8x12x30mm 4°

AVANOS

FDA UDI
Avanos Medical, Inc.·00193493934942·AVANOS* Single-Shot Epidural Trays

Halyard

FDA UDI
Avanos Medical, Inc.·10680651934946·HYH,EP TRY,S-SHOT,-,-,10

AED

FDA UDI
NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657016162·Hysteroscopy Continuous Flow Sheath, 2.9mm, 30*

Ophthalmic Retractor

FDA UDI
KATENA PRODUCTS, INC.·00841668100981·DESMARRES LID RETRACTOR #3

UniTip Catheter

FDA UDI
Unisensor AG·07640172973547·

BREEZE C MODEL C (3W), BREEZE C (4W)

FDA 510(k)
FDA Class 2 ·Physical Medicine

ROLL-X GUIDEWIRE

FDA 510(k)
FDA Class 2 ·Cardiovascular

BINAXNOW COVID-19 AG CARD

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·October 10, 2022

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 28, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 24, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 28, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·November 7, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·August 11, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 29, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 24, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 26, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·August 11, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·August 11, 2021