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FDA 510(k)

LacriPro Punctum Plug

K-Number: K161673 · 2016-11-18

ApplicantLacrimedics, Inc.
Decision Date2016-11-18
Product CodeLZU
DecisionSubstantially Equivalent

Device Summary

LacriPro Punctum Plug is the device name listed in this FDA 510(k) record. The listed applicant is Lacrimedics, Inc.. It received FDA 510(k) clearance on 2016-11-18 under 510(k) number K161673. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LacriPro Punctum Plug?

LacriPro Punctum Plug is a medical device that received FDA 510(k) clearance on 2016-11-18. The listed applicant is Lacrimedics, Inc.. The 510(k) number is K161673.

When did LacriPro Punctum Plug receive FDA 510(k) clearance?

LacriPro Punctum Plug received FDA 510(k) clearance on 2016-11-18, under 510(k) number K161673.

Who is the listed applicant for LacriPro Punctum Plug?

The FDA 510(k) record lists Lacrimedics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LacriPro Punctum Plug?

The FDA product code for LacriPro Punctum Plug is LZU.

Related Devices (Code: LZU)

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.

K241229Hello,eyes® BIO PlugBio Optics Co., Ltd.K222164Visant Medical Canalicular PlugVisant Medical, Inc.K213988SOFT PLUG Extended Duration 180 Tapered Canalicular PlugOasis Medical, Inc.K190210Tear Pool Dissolvable Punctum PlugsAlphamed, Inc.K162361Soft Plug Extended Duration 180 Canalicular PlugOasis Medical, Inc.

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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