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Sign in to claim this brandON-X LIFE TECHNOLOGIES, INC.
United States·US-MF-000026354
Last updated May 24, 2026
Information
- Country
- United States
- Address
- 1300 , East Anderson Lane Bldg B, Austin, United States
- Website
- www.artivion.com
- —
- —
- [email protected]
- Phone
- 770-419-3355
- PRRC Contact
- Drew Green
- EUDAMED SRN
- US-MF-000026354
- FDA FEI Number
- —
- DUNS Number
- 844782318
Catalogue (96)
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FDA Recalls (2)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Feb 1, 2026 | Z-2133-2026 | — | open, classified | Heart valves were released and distributed before all required testing was complete, so it cannot be confirmed that they meet all release specifications. |
| Dec 13, 2016 | Z-1057-2017 | — | terminated | Four issues were uncovered by the recalling firm's CAPA: 1) Burrs were found to be present on Left Housing, Right Housing and Barrel components, 2) Loose plastic particulate was found within sealed primary packages, 3) Loose hair was discovered within four sealed primary packages and 4) Assembly error, wherein Left and Right Housing components were acceptably press-fit together, was discovered within one sealed primary package. One of the Left Housing press-fit pins was not pressed into the associated hole of the Right Housing, resulting in a small gap in the housing assembly. |