34 results · 69ms · Sources: EU EUDAMED, US FDA

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DESIGN STANDARDS CORP.

FDA registration
DESIGN STANDARDS CORP.·20 products·🇺🇸 United States

VBAS Extension Arm

FDA UDI
DESIGN STANDARDS CORP.·00850003228075·Extension arm for use with the VYCOR Brain Acce...

SKIN STAPLER

FDA Adverse Event
Malfunction ·DESIGN STANDARDS CORP.·Product code GDT·October 10, 2019

SKIN STAPLER

FDA Adverse Event
Malfunction ·DESIGN STANDARDS CORP.·Product code GDT·August 27, 2020

CTS RELIEF KIT 4 EA

FDA Adverse Event
Injury ·DESIGN STANDARDS CORP·Product code MDM·August 30, 2021

PERMACLIP REEUSABLE HANDLE W/DISP. CLIP CART.

FDA Adverse Event
Malfunction ·DESIGN STANDARDS CORP·Product code FZP·July 25, 2008

PERMACLIP REUSABLE HANDLE W/DISP. CLIP

FDA Adverse Event
Malfunction ·DESIGN STANDARDS CORP·Product code GDO·July 25, 2008

PERMACLIP DISPOSABLE CARTRIDGE, 10MM CLIPS

FDA Adverse Event
Malfunction ·DESIGN STANDARDS CORP·Product code FZP·July 25, 2008

PERMACLIP DISPOSABLE CARTRIDGE, 10MM CLIPS

FDA Adverse Event
Injury ·DESIGN STANDARDS CORP·Product code FZP·July 30, 2008

PERMACLIP REUSABLE HANDLE W/DISP. CLIP CART

FDA Adverse Event
Injury ·DESIGN STANDARDS CORP·Product code GDO·July 30, 2008

PERMACLIP REUSABLE HANDLE W/DISP. CLIP CART

FDA Adverse Event
Injury ·DESIGN STANDARDS CORP·Product code FZP·July 30, 2008

CARPEL TUNNEL SYNDROME (CTS) RELIEF KIT

FDA Adverse Event
Injury ·DESIGN STANDARDS CORP·Product code MDM·March 26, 2021

CARPEL TUNNEL SYNDROME (CTS) RELIEF KIT

FDA Adverse Event
Injury ·DESIGN STANDARDS CORP·Product code MDM·January 19, 2021

CARPEL TUNNEL SYNDROME (CTS) RELIEF KIT

FDA Adverse Event
Injury ·DESIGN STANDARDS CORP·Product code MDM·January 14, 2021

PERMACLIP REUSABLE HDL. W/DISP. CLIP CARTRIDGE

FDA Adverse Event
Malfunction ·DESIGN STANDARDS CORP·Product code GDO·January 4, 2008

PERMACLIP DISPOSABLE CARTRIDGE 10MM CLIPS

FDA Adverse Event
Injury ·DESIGN STANDARDS CORP·Product code GDO·March 13, 2008

PERMACLIP REUSABLE HD1. W/DISP.CLIP CARTRIDGE

FDA Adverse Event
Malfunction ·DESIGN STANDARDS CORP·Product code GDO·January 4, 2008

LIFESYNC LEADWEAR

FDA Adverse Event
Other ·LIFESYNC CORPORATION·Product code DSA·January 9, 2009

MITROFLOW AORTIC PERICARDIAL HEART VALVE

FDA Adverse Event
Injury ·LIVANOVA CANADA CORP.·Product code DYE·October 28, 2016

GN RESOUND

FDA Adverse Event
Injury ·GN HEARING A/S·Product code OSM·September 21, 2022