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color contact lens;BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens

by Shenzhen Dashicheng Optical Technology Co., Ltd. 2 variants

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 Number06931219454961 UDI-DI Date17 Nov 2025ListedStatusListed 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  • Withdrawn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

Generic Name
Soft corrective contact lens, daily-wear
Model / Reference
BARBIE
Primary DI / UDI-DI
06931219454961
510(k) Number
FDA Product Code
LPL, MVN
GMDN Term
Soft corrective contact lens, daily-wear
Models / Variants
Device Class
Class II
Regulation Number
886.5925
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K220143)

Show all (12)

Other devices from Shenzhen Dashicheng Optical Technology Co., Ltd.

See all devices from Shenzhen Dashicheng Optical Technology Co., Ltd. →

Properties

  • Sterile
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

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