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KAOTIKLABS VE water based lubricant 5.3FL.OZ/150g

by Shenzhen Yongquan Medical Devices Co., Ltd.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06959633106396 UDI-DI Date7 May 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
KAOTIKLABS VE water based lubricant
Generic Name
Vaginal lubricant
Model / Reference
5.3FL.OZ/150g
Primary DI / UDI-DI
06959633106396
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
MRI Safety
MR Unsafe

Related devices

Cleared under the same submission (K251773)

Show all (12)

Other devices from Shenzhen Yongquan Medical Devices Co., Ltd.

See all devices from Shenzhen Yongquan Medical Devices Co., Ltd. →

Properties

  • Single Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No