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Lap-Band B-20401

by Apollo Endosurgery

Lap-Band B-20401 is a Class III device made by Apollo Endosurgery, listed in FDA GUDID since 12 Aug 2016 (UDI-DI 10811955020503), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10811955020503 UDI-DI Date12 Aug 2016ListedStatusListed GUDID: not in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Lap-Band
Generic name
Gastric band repair kit
Model / Ref / Catalog
B-20401
Primary DI / UDI-DI
10811955020503
FDA product code
LTI
GMDN term
Gastric band repair kit
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).

Other devices from Apollo Endosurgery

See all devices from Apollo Endosurgery →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Convenience kit
  • Lot / batch number
  • Serial number
  • Expiration date
Other properties (8, all answered No)