Teledyne Brown Engineering is one of 13048 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
2
Total
2
Cleared
0
Denied
Teledyne Brown Engineering, enables advanced technologies for air, land, sea, and space applications, with a manufacturing facility in Huntsville, US. The company has a history of developing specialized medical devices across multiple therapeutic areas.
Teledyne Brown Engineering received 2 FDA 510(k) clearances from 2 total submissions, with clearances spanning Anesthesiology and Physical Medicine device categories. The company's regulatory activity dates from 1995 to 1997. This company is inactive in the FDA 510(k) database and should be treated as a historical record.
Notable cleared devices include the TED 191 for anesthesiology applications and IMPERIUM for physical medicine. Explore the complete clearance history, device names, product codes, and clearance dates in the database.
FDA 510(k) Regulatory Record - Teledyne Brown Engineering
2 devices