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Aloe Cadabra BED2.9

by Live Well Brands, INC.

Aloe Cadabra BED2.9 is a vaginal lubricant (FDA Class II; FDA product code NUC, Lubricant, Personal) made by Live Well Brands, INC., cleared under FDA 510(k) K124044 on 30 Aug 2013 and listed in FDA GUDID since 8 Jun 2023 (UDI-DI 00826804004729), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K124044

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00826804004729 UDI-DI Date8 Jun 2023ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK124044 Date30 Aug 2013DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K124044 decided 30 Aug 2013 Active
  • FDA GUDID UDI-DI 00826804004729 listed 8 Jun 2023 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K124044
  2. Listed FDA GUDID 00826804004729

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Aloe Cadabra
Generic name
Vaginal lubricant
Model / reference
BED2.9
Primary DI / UDI-DI
00826804004729
510(k) Number
FDA product code
NUC
GMDN term
Vaginal lubricant
Device class
Class II
Regulation number
884.5300
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code NUC (Lubricant, Personal).

Other devices from Live Well Brands, INC.

See all devices from Live Well Brands, INC. →

Properties

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