DYNA INTRA-LIMBAL LENS
K-Number: K020006 · 2002-03-29
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Device Summary
Frequently Asked Questions
What is the DYNA INTRA-LIMBAL LENS?
DYNA INTRA-LIMBAL LENS is a medical device that received FDA 510(k) clearance on 2002-03-29. The listed applicant is Lens Dynamics, Inc.. The 510(k) number is K020006.
When did DYNA INTRA-LIMBAL LENS receive FDA 510(k) clearance?
DYNA INTRA-LIMBAL LENS received FDA 510(k) clearance on 2002-03-29, under 510(k) number K020006.
Who is the listed applicant for DYNA INTRA-LIMBAL LENS?
The FDA 510(k) record lists Lens Dynamics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DYNA INTRA-LIMBAL LENS?
The FDA product code for DYNA INTRA-LIMBAL LENS is HQD.
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.
Related Devices (Code: HQD)
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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