Well-Root ST
K-Number: K170950 · 2017-12-20
Device Summary
Frequently Asked Questions
What is the Well-Root ST?
Well-Root ST is a medical device that received FDA 510(k) clearance on 2017-12-20. The listed applicant is Vericom Co., Ltd.. The 510(k) number is K170950.
When did Well-Root ST receive FDA 510(k) clearance?
Well-Root ST received FDA 510(k) clearance on 2017-12-20, under 510(k) number K170950.
Who is the listed applicant for Well-Root ST?
The FDA 510(k) record lists Vericom Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Well-Root ST?
The FDA product code for Well-Root ST is KIF.
Other records listing Vericom 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: KIF)
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.