37 results
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27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Camber Sacroiliac (SI) Fixation System
FDA 510(k)
FDA Class 2
·Orthopedic
CosmeCore 50g Tip Package
FDA UDI
COSMEDENT, INC.·D77920350315·
Ophthalmic Cannula
FDA UDI
KATENA PRODUCTS, INC.·00841668114155·KRATZ POLISHER 23GA END (PK/10)
Ophthalmic Cannula
FDA UDI
KATENA PRODUCTS, INC.·00841668113783·AIR INJECT CANNULA 25GA
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756105651·CAST BOOT
Drive Rail
FDA UDI
ORTHOPEDIATRICS CORP.·00817867020283·Hinge, Low Overhang
Anatotemp
FDA UDI
BUCKEYE MEDICAL TECHNOLOGIES, LLC·D7862035030·Anatotemp Anatomic Dental Implant Healing Abutm...
SKINTACT ECG ELECTRODE
FDA 510(k)
FDA Class 2
·Cardiovascular
N LATEX CYSTATIN C
FDA 510(k)
FDA Class 2
·Clinical Chemistry
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