Contact Lens Case
K-Number: K171539 · 2017-07-14
Device Summary
Frequently Asked Questions
What is the Contact Lens Case?
Contact Lens Case is a medical device that received FDA 510(k) clearance on 2017-07-14. The listed applicant is E-Link Plastic & Metal Industrial Co.,Ltd. The 510(k) number is K171539.
When did Contact Lens Case receive FDA 510(k) clearance?
Contact Lens Case received FDA 510(k) clearance on 2017-07-14, under 510(k) number K171539.
Who is the listed applicant for Contact Lens Case?
The FDA 510(k) record lists E-Link Plastic & Metal Industrial Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Contact Lens Case?
The FDA product code for Contact Lens Case is LRX.
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.
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.