Company · US
Yukon Medical, LLC
FDA 510(k) clearances and medical device recalls filed under this name, 2012 to 2025. Name variants (Inc, Corp, punctuation) are merged.
11510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Mar 21, 2025 | K240761 | Arisure® Closed Male Luer with Spike Adapter (YM060) Yukon Medical, LLC | LHI |
| Dec 6, 2024 | K243486 | SmartSiteTM Vented Vial Access Device Yukon Medical, LLC | LHI |
| Mar 2, 2021 | K201422 | Arisure Closed System Drug Transfer Device (CSTD) Yukon Medical, LLC | ONB |
| Oct 3, 2017 | K172884 | Arisure Closed Vial Adapter Yukon Medical | LHI |
| Sep 29, 2017 | K172631 | Arisure Dry Spike Yukon Medical | LHI |
| Jun 2, 2017 | K171101 | Closed Male Luer Yukon Medical | FPA |
| Jul 31, 2015 | K151963 | SmartSite Vented Vial Access Device Yukon Medical, LLC | LHI |
| Oct 4, 2013 | K132863 | SMARTSITE VIALSHIELD Yukon Medical, LLC | LHI |
| Aug 14, 2012 | K122265 | VIALOK SINGLE VIAL ACCESS DEVICE VENTED Yukon Medical, LLC | LHI |
| May 3, 2012 | K121182 | VIALOK NON-VENTED Yukon Medical, LLC | LHI |
| Mar 30, 2012 | K120799 | ARISURE NEUTRAL VALVE Yukon Medical, LLC | FPA |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||