Greenway Yw, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Greenway Yw, LLC - FDA 510(k) Cleared Devices
Recent clearances: Apoller Flow Light Cure Flowable Composite
1
Total
1
Cleared
0
Denied
Greenway Yw, LLC has 1 FDA 510(k) cleared medical devices. Based in Lake Bluff, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Greenway Yw, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Iris Global, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Greenway Yw, LLC
1 devices