Dfine, Inc.
FDA 510(k) medical device clearances.
Top product codes for Dfine, Inc.
Recent clearances by Dfine, Inc.
- K091310 — ABLATION INSTRUMENT, MODEL 1635; ABLATION MULTIPLEX CATHETER, MODEL 1682
- K090986 — STABILI ERX BONE CEMENT, MODEL 1135,STABILIT VERTEBRAL AUGMENTATION SYSTEM (FOR USE W/ STABILIT ERX BONE CEMENT)
- K072496 — MODIFICATION TO SPACE CPSXL BONE CEMENT
- K070351 — SPACE 360 DELIVERY SYSTEM
- K061531 — SPACE CPSXL BONE CEMENT
Data sourced from openFDA. This site is unofficial and independent of the FDA.