Additive Device, Inc. (Adi) D/B/A Restor3D
Additive Device, Inc. (Adi) D/B/A Restor3D appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 5, 2019.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0