Medi Lift PLUS
K-Number: K220198 · 2023-06-28
Device Summary
Frequently Asked Questions
What is the Medi Lift PLUS?
Medi Lift PLUS is a medical device that received FDA 510(k) clearance on 2023-06-28. The listed applicant is Ya-Man, Ltd.. The 510(k) number is K220198.
When did Medi Lift PLUS receive FDA 510(k) clearance?
Medi Lift PLUS received FDA 510(k) clearance on 2023-06-28, under 510(k) number K220198.
Who is the listed applicant for Medi Lift PLUS?
The FDA 510(k) record lists Ya-Man, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Medi Lift PLUS?
The FDA product code for Medi Lift PLUS is NFO.
Other records listing Ya-Man, 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: NFO)
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.