Reshape Lifesciences

Reshape Lifesciences holds 4 FDA 510(k) medical device clearances, first cleared 2022, most recent 2024.

Top product codes for Reshape Lifesciences

KNT — Gastroenterology, Urology4 devices

Recent clearances by Reshape Lifesciences

K241039 — ReShape Calibration Tubes (B-2032, B-2036, B-2040) +2 moreCode KNT·2024-05-16
K230131 — ReShape Calibration TubesCode KNT·2023-02-15
K221898 — Gastrointestinal Boundary Identifier (GIBI HD)Code KNT·2022-07-28
K220455 — Lap-Band System Calibration TubeCode KNT·2022-06-07

Data sourced from openFDA. This site is unofficial and independent of the FDA.