Roosin Collagen Powder
K-Number: K254034 · 2026-06-03
Device Summary
Frequently Asked Questions
What is the Roosin Collagen Powder?
Roosin Collagen Powder is a medical device that received FDA 510(k) clearance on 2026-06-03. The listed applicant is Roosin Medical Co., Ltd.. The 510(k) number is K254034.
When did Roosin Collagen Powder receive FDA 510(k) clearance?
Roosin Collagen Powder received FDA 510(k) clearance on 2026-06-03, under 510(k) number K254034.
Who is the listed applicant for Roosin Collagen Powder?
The FDA 510(k) record lists Roosin Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Roosin Collagen Powder?
The FDA product code for Roosin Collagen Powder is KGN.
Other records listing Roosin Medical Co., 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: KGN)
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.