Indigo Orb, Inc. is one of 25313 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Indigo Orb, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AUTODETECT SYRINGE
1
Total
1
Cleared
0
Denied
Indigo Orb, Inc. has 1 FDA 510(k) cleared medical devices. Based in Santa Clara, US.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Indigo Orb, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Indigo Orb, Inc.
1 devices