638 results
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41ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Teleflex LLC
FDA registration
Teleflex LLC·3 products·🇺🇸 United States
Teleflex Medical LLC
FDA registration
Teleflex Medical LLC·547 products·🇺🇸 United States
Teleflex LLC (NADC)
FDA registration
Teleflex LLC (NADC)·463 products·🇺🇸 United States
Teleflex Medical LLC
FDA registration
Teleflex Medical LLC·15 products·🇺🇸 United States
Teleflex Medical LLC
FDA registration
Teleflex Medical LLC·2 products·🇺🇸 United States
Teleflex Medical OEM LLC
FDA registration
Teleflex Medical OEM LLC·8 products·🇺🇸 United States
Arrow International, LLC (subsidiary of Teleflex Incorporated)
FDA registration
Arrow International, LLC (subsidiary of Teleflex Incorporated)·49 products·🇺🇸 United States
Arrow International, LLC (subsidiary of Teleflex, Incorporated)
FDA registration
Arrow International, LLC (subsidiary of Teleflex, Incorporated)·11 products·🇺🇸 United States
Arrow International LLC (subsidiary of Teleflex Incorporated)
FDA registration
Arrow International LLC (subsidiary of Teleflex Incorporated)·27 products·🇺🇸 United States
SKIN STAPLER 35W
FDA Adverse Event
Injury
·TELEFLEX LLC·Product code QQS·December 23, 2025
MICRO PUNCTURE KIT
FDA Adverse Event
Injury
·TELEFLEX LLC·Product code DYB·August 1, 2024
SKIN STAPLER 35W
FDA Adverse Event
Injury
·TELEFLEX LLC·Product code QQS·August 9, 2024
SKIN STAPLER 35W
FDA Adverse Event
Injury
·TELEFLEX LLC·Product code QQS·August 9, 2024
SKIN STAPLER 35W
FDA Adverse Event
Injury
·TELEFLEX LLC·Product code QQS·August 9, 2024
SKIN STAPLER 35W
FDA Adverse Event
Injury
·TELEFLEX LLC·Product code QQS·August 9, 2024
HUDSON RCI
FDA Adverse Event
Malfunction
·TELEFLEX LLC·Product code BTR·July 3, 2023
VASCBAND
FDA Adverse Event
Malfunction
·TELEFLEX LLC.·Product code DXC·November 4, 2024
WECK
FDA Adverse Event
Malfunction
·TELEFLEX, LLC·Product code HAO·January 29, 2026
BITEGARD BITE BLOCK
FDA Adverse Event
Malfunction
·TELEFLEX LLC·Product code BRW·March 25, 2025
Teleflex HORIZON Microclip Titanium Ligating Clips w/tape, REF 005200; for use in general surgical procedures that require vessel or tissue ligation
FDA Enforcement
Class II
·Ongoing·TELEFLEX LLC·June 7, 2023