Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses

K-Number: K173136 · 2017-11-16

ApplicantMenicon Co, Ltd.
Decision Date2017-11-16
Product CodeMRC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses is the device name listed in this FDA 510(k) record. The listed applicant is Menicon Co, Ltd.. It received FDA 510(k) clearance on 2017-11-16 under 510(k) number K173136. The device is classified under product code MRC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses?

Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses is a medical device that received FDA 510(k) clearance on 2017-11-16. The listed applicant is Menicon Co, Ltd.. The 510(k) number is K173136.

When did Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses receive FDA 510(k) clearance?

Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses received FDA 510(k) clearance on 2017-11-16, under 510(k) number K173136.

Who is the listed applicant for Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses?

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

What is the FDA product code for Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses?

The FDA product code for Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses is MRC.

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.

NCT07494799Efficacy of Different Interventions for Progressive Myopia After Orthokeratology Lens WearNOT_YET_RECRUITINGNCT07288658Comparing the Fit and Performance of Scleral Lenses With Oval and Circular Limbal ZonesCOMPLETED

Other records listing Menicon Co, Ltd. as applicant

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.

K253795MeniSept 3% Hydrogen Peroxide Cleaning & Disinfecting SolutionPMA P990018Lens, contact (rigid gas permeable), extended wearK193399Miru 1day UpSide (midafilcon A)K191872Menicon 3% Hydrogen Peroxide Cleaning and Disinfecting SolutionK180819One Day Flat Pack (hioxifilcon A) Daily Disposable Soft Contact LensK180004Menicon ASRB (asmofilcon A) Silicone Hydrogel Soft Contact Lens

View all 7 devices →

Related Devices (Code: MRC)

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.

K251876cleadew GP hydra oneOphtecs CorporationK200416Boston One Step Liquid Enzymatic CleanerBausch & Lomb, IncorporatedK201069VibrantVue Scleral SalineDry Eye Innovations, LLCK182984MaxiTears Contacts PFOmnivision AGK181566NutrifillContamac, Ltd.K181627Bausch + Lomb Boston SimplusMulti-Action Solution, Bausch + Lomb Boston One Step Liquid Enzymatic CleanerBausch & Lomb, Incorporated

Official Source

View on FDA Database →

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

↑