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

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

MEDO-Thyroid

FDA 510(k)
FDA Class 2 ·Radiology

Lockheed - 18 Metal

FDA UDI
Certified Safety Manufacturing, Inc.·00766588015026·Lockheed - 18 Metal

Marking Pen

FDA UDI
KATENA PRODUCTS, INC.·00841668114384·MARKING PEN MICRO (PK/10)

DeRoyal

FDA UDI
DEROYAL INDUSTRIES, INC.·00749756105637·CAST BOOT

Anatotemp

FDA UDI
BUCKEYE MEDICAL TECHNOLOGIES, LLC·D7862035020·Anatotemp Anatomic Dental Implant Healing Abutm...

Drive Rail

FDA UDI
ORTHOPEDIATRICS CORP.·00817867020276·Hinge, High Range

JEWEL CAST PLUS

FDA 510(k)
FDA Class 2 ·Dental

CELLSEARCH CIRCULATING TUMOR CELL KIT MODEL 7900001

FDA 510(k)
FDA Class 2 ·Immunology

ARI Anterior Staple System

FDA UDI
VB Spine LLC·10888857235755·Removable Fork Distractor Tip (Right)

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·July 7, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·September 9, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·July 8, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·July 8, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·July 8, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·July 8, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·August 17, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·September 1, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·July 8, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·August 4, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·September 23, 2022