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Yukon Medical, LLC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30096316693009631669Yukon Medical, LLC1N2026-01-014021 Stirrup Creek Dr Ste 200 Durham NC US 27703

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00851891007070ViaLok - 13mm ViaLok V Vented Vial Access Device919-595-8250Quality@YukonMedical.com
00851891007292Arisure - Arisure CML with Spike Adapter919-595-8250Quality@YukonMedical.com
00851891007308Arisure - Arisure Bag Spike919-595-8250Quality@YukonMedical.com
00851891007605Arisure - Arisure Spike Adapter with CML919-595-8250Quality@YukonMedical.com
00851891007629Arisure - Vented Bag Spike919-595-8250Quality@YukonMedical.com
10851891007299Arisure - Arisure CML with Spike Adapter919-595-8250Quality@YukonMedical.com
20851891007609Arisure - Arisure Spike Adapter with CML919-595-8250Quality@YukonMedical.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1448871887000953K243486SmartSiteTM Vented Vial Access DeviceLHI2024-12-06
1448871641105505K240761Arisure® Closed Male Luer with Spike Adapter (YM060)LHI2025-03-21
1448871860899907K201422Arisure Closed System Drug Transfer Device (CSTD)ONB2021-03-02
1448871713666246K172884Arisure Closed Vial AdapterLHI2017-10-03
1448871203962263K172631Arisure Dry SpikeLHI2017-09-29
1448871905565753K171101Closed Male LuerFPA2017-06-02
1448871194607547K151963SmartSite Vented Vial Access DeviceLHI2015-07-31
1448871278353425K132863SMARTSITE VIALSHIELDLHI2013-10-04
1448871161459233K122265VIALOK SINGLE VIAL ACCESS DEVICE VENTEDLHI2012-08-14
1448871259065173K121182VIALOK NON-VENTEDLHI2012-05-03
1448871671957822K120799ARISURE NEUTRAL VALVEFPA2012-03-30
1448871057420649

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
LHI82025-03-21
FPA22017-06-02
ONB12021-03-02

PMN#

GUDID#

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