TORIC LITE LENS
K-Number: K011256 · 2001-07-17
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Device Summary
Frequently Asked Questions
What is the TORIC LITE LENS?
TORIC LITE LENS is a medical device that received FDA 510(k) clearance on 2001-07-17. The listed applicant is Soflex Contact Lens Industries , Ltd.. The 510(k) number is K011256.
When did TORIC LITE LENS receive FDA 510(k) clearance?
TORIC LITE LENS received FDA 510(k) clearance on 2001-07-17, under 510(k) number K011256.
Who is the listed applicant for TORIC LITE LENS?
The FDA 510(k) record lists Soflex Contact Lens Industries , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TORIC LITE LENS?
The FDA product code for TORIC LITE 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 Soflex Contact Lens Industries , 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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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