CapsoVision, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K252480CE Deliver (DLV)December 19, 2025
K242643CapsoCam Plus (SV-3) Capsule Endoscopy SystemDecember 4, 2024
K192662CapsoCam Plus (SV-3) Capsule Endoscopy SystemFebruary 14, 2020
K183192CapsoCam Plus (SV-3)April 19, 2019
K161773CapsoCam Plus (SV-3) Capsule Endoscope SystemOctober 21, 2016
K151635CapsoCam (SV-1)February 9, 2016