Home › Device types › FWW
Table, Operating-Room, Pneumatic
FDA product code FWW · Class 1 · General, Plastic Surgery
22
Registered devices
26
Adverse events
0
Recalls
6
510(k) clearances
Devices with this code
ATEC A.R.M. — ALPHATEC SPINE, INC.ATEC A.R.M. — ALPHATEC SPINE, INC.ATEC A.R.M. — ALPHATEC SPINE, INC.Amsco — STERIS CORPORATIONATEC A.R.M. — ALPHATEC SPINE, INC.ATEC A.R.M. — ALPHATEC SPINE, INC.ATEC A.R.M. — ALPHATEC SPINE, INC.ATEC A.R.M. — ALPHATEC SPINE, INC.ATEC A.R.M. — ALPHATEC SPINE, INC.ATEC A.R.M. — ALPHATEC SPINE, INC.ATEC A.R.M. — ALPHATEC SPINE, INC.ATEC A.R.M. — ALPHATEC SPINE, INC.ATEC A.R.M. — ALPHATEC SPINE, INC.ATEC A.R.M. — ALPHATEC SPINE, INC.ATEC A.R.M. — ALPHATEC SPINE, INC.ATEC A.R.M. — ALPHATEC SPINE, INC.ATEC A.R.M. — ALPHATEC SPINE, INC.ATEC A.R.M. — ALPHATEC SPINE, INC.ATEC A.R.M. — ALPHATEC SPINE, INC.ATEC A.R.M. — ALPHATEC SPINE, INC.ATEC A.R.M. — ALPHATEC SPINE, INC.ATEC A.R.M. — ALPHATEC SPINE, INC.
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
