Restor3D
Restor3D holds FDA 510(k) medical device clearances, first cleared 2020, most recent 2026.
Top product codes for Restor3D
Recent clearances by Restor3D
- K260556 — Veritas Shoulder System
- K253992 — Veritas Reverse Total Shoulder System
- K252454 — Kinos Total Ankle System
- K243643 — restor3d Reverse Total Shoulder Arthroplasty System
- K242868 — Kinos Total Ankle System
- K241482 — Kinos Total Ankle System
- K234087 — restor3d TIDAL Lumbar Interbody Fusion System
- K232595 — Kinos Axiom Total Ankle System
- K231458 — Extremity Staple
- K223326 — Axiom PSR System
- K220523 — restor3d TiDAL Lumbar Interbody Fusion Device
- K211789 — restor3d Pin Implants
- K193491 — restor3d Metallic Interference Screw
Data sourced from openFDA. This site is unofficial and independent of the FDA.