Lap-Band B-2017
Lap-Band B-2017 is a Class III device made by Apollo Endosurgery, listed in FDA GUDID since 12 Aug 2016 (UDI-DI 10811955020374), not in commercial distribution (GUDID) as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10811955020374 | Date12 Aug 2016 | StatusListed |
Official records
- AccessGUDID record 10811955020374
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Lap-Band
- Generic name
- Gastric calibration tube
- Model / Ref / Catalog
- B-2017
- Primary DI / UDI-DI
- 10811955020374
- FDA product code
- LTI
- GMDN term
- Gastric calibration tube
- Device class
- Class III
- GUDID distribution status
- Not in Commercial Distribution
Similar devices
Other devices filed under FDA product code LTI (Implant, Intragastric For Morbid Obesity).
- Garren Gastric Bubble by American Edwards Laboratories
- Realize Adjustable Gastric Band Model 2200-X with Injection Port & Applier by Obtech Medical GmbH
- Lap-Band Adjustable Gastric Banding System by Medtimo, Inc.
- Reshape Integrated Dual Balloon System by Boston Scientific
- TransPyloric Shuttle Delivery Device by Baronova, Inc.
- Allurion Gastric Balloon System by Allurion Technologies Inc.
- ORBERA Intragastric Balloon System by Boston Scientific
- Spatz3 Adjustable Balloon System by Spatz Fgia, Inc.
- Obalon Touch Inflation System by Medtimo, Inc.