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FDA 510(k)

Visant Medical Canalicular Plug

K-Number: K222164 · 2022-12-23

ApplicantVisant Medical, Inc.
Decision Date2022-12-23
Product CodeLZU
DecisionSubstantially Equivalent

Device Summary

Visant Medical Canalicular Plug is the device name listed in this FDA 510(k) record. The listed applicant is Visant Medical, Inc.. It received FDA 510(k) clearance on 2022-12-23 under 510(k) number K222164. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Visant Medical Canalicular Plug?

Visant Medical Canalicular Plug is a medical device that received FDA 510(k) clearance on 2022-12-23. The listed applicant is Visant Medical, Inc.. The 510(k) number is K222164.

When did Visant Medical Canalicular Plug receive FDA 510(k) clearance?

Visant Medical Canalicular Plug received FDA 510(k) clearance on 2022-12-23, under 510(k) number K222164.

Who is the listed applicant for Visant Medical Canalicular Plug?

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

What is the FDA product code for Visant Medical Canalicular Plug?

The FDA product code for Visant Medical Canalicular 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.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.K161673LacriPro Punctum PlugLacrimedics, 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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