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NHS INC

FDA registration
NHS INC·1 product·🇺🇸 United States

NHS 2009SP HEARING AID

FDA 510(k)
FDA Class 1 ·Ear, Nose, Throat

ALARA Neuro Access Needle Kit

FDA UDI
SURGENTEC, LLC·00858406007334·ALARA Neuro Access Needle Kit with Extension Ha...

ALARA Neuro Access Needle Kit

FDA UDI
SURGENTEC, LLC·00858406007341·ALARA Neuro Access Needle Kit with Extension Ha...

NHS 2044P BODY AID, HEARING AID

FDA 510(k)
FDA Class 1 ·Ear, Nose, Throat

NHS Scotland Cataract Set Rayner 74

FDA UDI
Hasa Optix·05404027449470·

COAT-A-COUNT NHS-PROLACTIN KIT AND

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

UNK GEL BREAST IMPLANT

FDA Adverse Event
Injury ·ALLERGAN (COSTA RICA)·Product code FTR·August 13, 2023

NAIL HOLDING SCREW GAMMA3® 8X35MM

FDA Adverse Event
Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·July 12, 2017

NAIL HOLDING SCREW GAMMA3® 8X35MM

FDA Adverse Event
Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·December 17, 2015

TARGET DEVICE GAMMA3® 300X160MM

FDA Adverse Event
Malfunction ·STRYKER TRAUMA KIEL·Product code HSB·December 17, 2015

NAIL HOLDING SCREW GAMMA3 8X35MM

FDA Adverse Event
Malfunction ·STRYKER OSTEOSYNTHESIS-KIEL·Product code LXH·April 12, 2013

NAIL HANDLE T2 TIBIA

FDA Adverse Event
Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·July 22, 2014

NAIL HOLDING SCREW, TIBIA T2 TIBIA 10 MM

FDA Adverse Event
Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·July 22, 2014

NAIL HANDLE T2 TIBIA

FDA Adverse Event
Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·July 11, 2016

NAIL HOLDING SCREW, TIBIA T2 TIBIA 10 MM

FDA Adverse Event
Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·July 11, 2016

NAIL HOLDING SCREW GAMMA3® 8X35MM

FDA Adverse Event
Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·September 26, 2016

SPEEDLOCK SLEEVE GAMMA3® 180

FDA Adverse Event
Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·June 23, 2016

NAIL HOLDING SCREW, TIBIA T2 TIBIA 10 MM

FDA Adverse Event
Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·June 27, 2016

6F ANGIO-SEAL VIP VASCULAR CLOSURE DEVICE, OUS

FDA Adverse Event
Malfunction ·TERUMO MEDICAL CORPORATION·Product code MGB·September 17, 2023