CapsoVision, Inc.
CapsoVision, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 19, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K252480 | CE Deliver (DLV) | December 19, 2025 |
| K242643 | CapsoCam Plus (SV-3) Capsule Endoscopy System | December 4, 2024 |
| K192662 | CapsoCam Plus (SV-3) Capsule Endoscopy System | February 14, 2020 |
| K183192 | CapsoCam Plus (SV-3) | April 19, 2019 |
| K161773 | CapsoCam Plus (SV-3) Capsule Endoscope System | October 21, 2016 |
| K151635 | CapsoCam (SV-1) | February 9, 2016 |