Eye Recovery Pro (PH-e03)
K-Number: K261602 · 2026-08-10
Device Summary
Frequently Asked Questions
What is the Eye Recovery Pro (PH-e03)?
Eye Recovery Pro (PH-e03) is a medical device that received FDA 510(k) clearance on 2026-08-10. The listed applicant is Shenzhen Goodwind Technology Development Co., Ltd.. The 510(k) number is K261602.
When did Eye Recovery Pro (PH-e03) receive FDA 510(k) clearance?
Eye Recovery Pro (PH-e03) received FDA 510(k) clearance on 2026-08-10, under 510(k) number K261602.
Who is the listed applicant for Eye Recovery Pro (PH-e03)?
The FDA 510(k) record lists Shenzhen Goodwind Technology Development Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Eye Recovery Pro (PH-e03)?
The FDA product code for Eye Recovery Pro (PH-e03) is OHS.
Other records listing Shenzhen Goodwind Technology Development 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: OHS)
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.