Neptune Medical, Inc.
Neptune Medical, Inc. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 18, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K262262 | Pathfinder Endoscope Overtube | September 18, 2026 |
| K260503 | Triton 1 System | September 3, 2026 |
| K240853 | Pathfinder® CR System | June 27, 2024 |
| K230801 | Pathfinder Endoscope Overtube with Balloon Device | July 28, 2023 |
| K211301 | Pathfinder Endoscope Overtube | May 28, 2021 |
| K210915 | Pathfinder Endoscope Cap | May 25, 2021 |
| K191415 | Pathfinder Endoscope Overtube | August 30, 2019 |