VEA Align
K-Number: K231917 · 2024-01-05
Device Summary
Frequently Asked Questions
What is the VEA Align?
VEA Align is a medical device that received FDA 510(k) clearance on 2024-01-05. The listed applicant is Eos Imaging. The 510(k) number is K231917.
When did VEA Align receive FDA 510(k) clearance?
VEA Align received FDA 510(k) clearance on 2024-01-05, under 510(k) number K231917.
Who is the listed applicant for VEA Align?
The FDA 510(k) record lists Eos Imaging as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VEA Align?
The FDA product code for VEA Align is QIH.
Other records listing Eos Imaging 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: QIH)
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.