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Aloe Cadabra AP15

by Live Well Brands, INC.

Aloe Cadabra AP15 is a vaginal applicator (FDA Class I; FDA product code HGD, Applicator, Vaginal) made by Live Well Brands, INC., listed in FDA GUDID since 16 Jun 2023 (UDI-DI 00826804006938), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

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 Number00826804006938 UDI-DI Date16 Jun 2023ListedStatusListed GUDID: 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  • Withdrawn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
Aloe Cadabra
Generic name
Vaginal applicator, single-use
Model / reference
AP15
Primary DI / UDI-DI
00826804006938
FDA product code
HGD
GMDN term
Vaginal applicator, single-use
Device class
Class I
Regulation number
884.4520
GUDID distribution status
In Commercial Distribution

Related devices

Category: Vaginal applicator, single-use

Other devices from Live Well Brands, INC.

See all devices from Live Well Brands, INC. →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)