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FDA 510(k)

BENZ-G 4X (HIOXIFILCON D) MULTIFOCAL LATHED LENS

K-Number: K101122 · 2010-08-09

Decision Date2010-08-09
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BENZ-G 4X (HIOXIFILCON D) MULTIFOCAL LATHED LENS is the device name listed in this FDA 510(k) record. The listed applicant is Benz Research and Development Corp.. It received FDA 510(k) clearance on 2010-08-09 under 510(k) number K101122. 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 BENZ-G 4X (HIOXIFILCON D) MULTIFOCAL LATHED LENS?

BENZ-G 4X (HIOXIFILCON D) MULTIFOCAL LATHED LENS is a medical device that received FDA 510(k) clearance on 2010-08-09. The listed applicant is Benz Research and Development Corp.. The 510(k) number is K101122.

When did BENZ-G 4X (HIOXIFILCON D) MULTIFOCAL LATHED LENS receive FDA 510(k) clearance?

BENZ-G 4X (HIOXIFILCON D) MULTIFOCAL LATHED LENS received FDA 510(k) clearance on 2010-08-09, under 510(k) number K101122.

Who is the listed applicant for BENZ-G 4X (HIOXIFILCON D) MULTIFOCAL LATHED LENS?

The FDA 510(k) record lists Benz Research and Development Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BENZ-G 4X (HIOXIFILCON D) MULTIFOCAL LATHED LENS?

The FDA product code for BENZ-G 4X (HIOXIFILCON D) MULTIFOCAL LATHED 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.

Other records listing Benz Research and Development Corp. 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.

View all 12 devices →

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.

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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