Yukon Medical, LLC
Yukon Medical, LLC appears in FDA public data with 0 recalls, 11 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 21, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 11
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K240761 | Arisure® Closed Male Luer with Spike Adapter (YM060) | March 21, 2025 |
| K243486 | SmartSiteTM Vented Vial Access Device | December 6, 2024 |
| K201422 | Arisure Closed System Drug Transfer Device (CSTD) | March 2, 2021 |
| K172884 | Arisure Closed Vial Adapter | October 3, 2017 |
| K172631 | Arisure Dry Spike | September 29, 2017 |
| K171101 | Closed Male Luer | June 2, 2017 |
| K151963 | SmartSite Vented Vial Access Device | July 31, 2015 |
| K132863 | SMARTSITE VIALSHIELD | October 4, 2013 |
| K122265 | VIALOK SINGLE VIAL ACCESS DEVICE VENTED | August 14, 2012 |
| K121182 | VIALOK NON-VENTED | May 3, 2012 |
| K120799 | ARISURE NEUTRAL VALVE | March 30, 2012 |