Reshape Lifesciences

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
5
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K241039ReShape Calibration Tubes (B-2032, B-2036, B-2040); ReShape Calibration Tubes (B-2017); Gastric BallMay 16, 2024
K230131ReShape Calibration TubesFebruary 15, 2023
K221898Gastrointestinal Boundary Identifier (GIBI HD)July 28, 2022
K220455Lap-Band System Calibration TubeJune 7, 2022