Seedling Enterprises., LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Seedling Enterprises., LLC - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Seedling Enterprises., LLC has 4 FDA 510(k) cleared medical devices. Based in Ayer, US.
Historical record: 4 cleared submissions from 2000 to 2001. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Seedling Enterprises., LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Seedling Enterprises., LLC
4 devices
Cleared
Sep 20, 2001
MULTIFUNCTION ENDOSCOPIC INSTRUMENT
General & Plastic Surgery
83d
Cleared
May 18, 2001
SEEDLING ENTERPRISES LLC, COOL TEC MONOPOLAR AND BIPOLAR REUSABLE ELECTRODES
General & Plastic Surgery
70d
Cleared
Dec 08, 2000
COOL-TEC ELECTRODES
General & Plastic Surgery
87d
Cleared
Jul 19, 2000
COOL-TEC ELECTRODES
General & Plastic Surgery
43d