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Lap-Band B-20302

by Apollo Endosurgery

Lap-Band B-20302 is a Class III device made by Apollo Endosurgery, listed in FDA GUDID since 17 Aug 2016 (UDI-DI 10811955020428), 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 Number10811955020428 UDI-DI Date17 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  • Withdrawn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
Subcutaneous infusion/injection port needle
Model / Ref / Catalog
B-20302
Primary DI / UDI-DI
10811955020428
FDA product code
LTI
GMDN term
Subcutaneous infusion/injection port needle
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
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)