47 results
·
35ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Spok, Inc. Plano Division
FDA registration
Spok, Inc. Plano Division·1 product·🇺🇸 United States
Messenger
FDA UDI
SPOK INC.·00865190000304·Messenger 5.18 Software Release
Messenger
FDA UDI
SPOK INC.·00860011811961·Messenger 6.1.1 Software Release
Messenger
FDA UDI
SPOK INC.·00860011811909·Messenger 5.17.16 Software Release
Messenger
FDA UDI
SPOK INC.·00860011811916·Messenger 5.18.2 Software Release
Messenger
FDA UDI
SPOK INC.·00860011811947·Messenger 5.17.17 Software Release
Messenger
FDA UDI
SPOK INC.·00860011811930·Messenger 5.18.3 Software Release
Messenger
FDA UDI
SPOK INC.·00860011811923·Messenger 6.1.0 Software Release
Messenger
FDA UDI
SPOK INC.·00860011425502·Messenger 6.0.0 Software Release
Messenger
FDA UDI
SPOK INC.·00860011811954·Messenger 5.18.4 Software Release
STAPLER 45 RELOAD, BLUE
FDA Adverse Event
Injury
·INTUITIVE SURGICAL,INC.·Product code NAY·September 28, 2017
SPOT HEALTH INC.
FDA registration
SPOT HEALTH INC.·9 products·🇺🇸 United States
GUT CHR UD 18IN 6-0 D/A G-1 PRM
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAL·August 29, 2025
SUTURE UNKNOWN
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAK·August 29, 2025
V-GO DISPOSABLE INSULIN DELIVERY DEVICE
FDA Adverse Event
Malfunction
·MANNKIND CORPORATION - V-GO·Product code LZG·June 24, 2022
THERMOCOOL SMARTTOUCH SF
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code LPB·April 10, 2025
OUTLOOK®
FDA Adverse Event
Malfunction
·B. BRAUN DOMINICAN REPUBLIC INC.·Product code FPA·November 29, 2016
BLOOD ADMINISTRATION SET
FDA Adverse Event
Malfunction
·B. BRAUN DOMINICAN REPUBLIC INC.·Product code FPA·November 23, 2016
6F PRELUDE + NEEDLE SHEATH INTRODUCER
FDA Adverse Event
Injury
·MERIT MEDICAL SYSTEMS, INC.·Product code DRE·October 16, 2023
6F PRELUDE + NEEDLE SHEATH INTRODUCER
FDA Adverse Event
Injury
·MERIT MEDICAL SYSTEMS, INC.·Product code DRE·October 16, 2023