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FDA 510(k)

BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens

K-Number: K220143 · 2022-09-08

ApplicantShenzhen Dashicheng Optical Technology Co., Ltd.
Decision Date2022-09-08
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Dashicheng Optical Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-09-08 under 510(k) number K220143. The device is classified under product code LPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens?

BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens is a medical device that received FDA 510(k) clearance on 2022-09-08. The listed applicant is Shenzhen Dashicheng Optical Technology Co., Ltd.. The 510(k) number is K220143.

When did BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens receive FDA 510(k) clearance?

BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens received FDA 510(k) clearance on 2022-09-08, under 510(k) number K220143.

Who is the listed applicant for BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens?

The FDA 510(k) record lists Shenzhen Dashicheng Optical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens?

The FDA product code for BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens is LPL.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT04840563Surface Refractive Index Shift of Kalifilcon A Compared With Dailies Total1 and Precision1 LensesCOMPLETEDNCT05285527MiSight 1 Day Safety Post-Approval StudyACTIVE_NOT_RECRUITINGNCT06751225Evaluation of Wear Experience With a Weekly Replacement Soft Contact Lens in Neophyte Lens Wearers With AstigmatismCOMPLETEDNCT07747311Contact Lenses to Slow Myopia Progression in AdultsNOT_YET_RECRUITINGNCT053259311-Week Dispensing Evaluation of Kalifilcon A Daily Disposable Multifocal Compared to Ultra for PresbyopiaCOMPLETEDNCT06749496Evaluation of Delefilcon A and Senofilcon A Daily Disposable Toric Soft Contact Lenses Over One Week of WearCOMPLETED

Related Devices (Code: LPL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260507Interojo 45 (inofilcon A) Soft (Hydrophilic) Silicone Hydrogel Contact Lens with GrabSoo PlusINTEROJO, Inc.K253352Pegavision (Polymacon) Daily Disposable Soft (Hydrophilic) Contact Lenses; Pegavision (Polymacon) Soft (Hydrophilic) Contact Lenses; Pegavision (Polymacon) Color Daily Disposable Soft (Hydrophilic) Contact Lenses; Pegavision (Polymacon) Color Soft (Hydrophilic) Contact LensesPegavision CorporationK261299Pegavision (Toufilcon B) Daily Disposable Soft (Hydrophilic) Contact Lenses; Pegavision (Toufilcon B) Soft (Hydrophilic) Contact LensesPegavision CorporationK253885PUSCON WATER BALANCE-1DAY TINT (omafilcon A) SOFT (HYDROPHILIC) CONTACT LENS; PUSCON WATER BALANCE-1DAY COLOR (omafilcon A) SOFT (HYDROPHILIC) CONTACT LENSESGEO MEDICAL CO., LTD.K254269Saview SH Optic 38 UV (Senofilcon A) Visibility Tinted Soft (Hydrophilic) Contact Lens; Saview SH Optic 38 UV toric (Senofilcon A) Visibility Tinted Soft (Hydrophilic) Contact Lens; Saview SH Optic 38 UV multifocal (Senofilcon A) Visibility Tinted Soft (Hydrophilic) Contact LensSt. shine Optical Co., Ltd.K252385Pegavision (Toufilcon B) Daily Disposable Soft (Hydrophilic) Contact Lenses; Pegavision (Toufilcon B) Soft (Hydrophilic) Contact LensesPegavision Corporation

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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