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 NECT CONTACT LENS CASE

K-Number: K131875 · 2013-08-06

ApplicantForesight Regulatory Strategies
Decision Date2013-08-06
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MENICON NECT CONTACT LENS CASE is the device name listed in this FDA 510(k) record. The listed applicant is Foresight Regulatory Strategies. It received FDA 510(k) clearance on 2013-08-06 under 510(k) number K131875. The device is classified under product code LRX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MENICON NECT CONTACT LENS CASE?

MENICON NECT CONTACT LENS CASE is a medical device that received FDA 510(k) clearance on 2013-08-06. The listed applicant is Foresight Regulatory Strategies. The 510(k) number is K131875.

When did MENICON NECT CONTACT LENS CASE receive FDA 510(k) clearance?

MENICON NECT CONTACT LENS CASE received FDA 510(k) clearance on 2013-08-06, under 510(k) number K131875.

Who is the listed applicant for MENICON NECT CONTACT LENS CASE?

The FDA 510(k) record lists Foresight Regulatory Strategies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MENICON NECT CONTACT LENS CASE?

The FDA product code for MENICON NECT CONTACT LENS CASE is LRX.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Related Devices (Code: LRX)

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.

K252175LANDR Contact LENS CaseFourth Axis, LLCK250495MINI VP1 (PL67_F); MINI VP1 (PL61_F)Avizor S.A.K240095CAREUS Contact Lens Case (Model 1, Model 2, Model 3, Model 4, Model 5, Model 6)Shanghai Care US Medical Product Co., Ltd.K231123Phoenix Contact Lens Case - dome top flat pack (CL-01); Phoenix Contact Lens Case - classic flat pack (CL-02); Phoenix Contact Lens Case - sunglass shape flat pack (CL-03)Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd.K173538Clear Care Cleaning & Disinfecting Solution, AOCup Lens Case with AODiscAlcon Laboratories, Inc.K172925Contact Lens Case, Model: A-1, B-1P L Overseas Limited

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.

↑