Rhino Health, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rhino Health, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Rhino Non-sterile Powder-Free Nitrile Exam Glove – Periwinkle Color Tested for Use with Chemotherapy Drugs and Fentanyl, Rhino Non-Sterile, Powder-Free Nitrile Exam Gloves – Periwinkle Color Tested for Use with Chemotherapy Drugs, and Fentanyl, Rhino Health Non-Sterile, Powder-free Nitrile Exam Glove
3
Total
3
Cleared
0
Denied
Rhino Health, Inc. has 3 FDA 510(k) cleared medical devices. Based in Church Rock, US.
Last cleared in 2023. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Rhino Health, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Capote Law Firm and Global Regulatory Partners, Inc..
FDA 510(k) Regulatory Record - Rhino Health, Inc.
3 devices
Cleared
Feb 13, 2023
Rhino Non-sterile Powder-Free Nitrile Exam Glove – Periwinkle Color Tested...
General Hospital
52d
Cleared
Nov 30, 2022
Rhino Non-Sterile, Powder-Free Nitrile Exam Gloves – Periwinkle Color Tested...
General Hospital
231d
Cleared
Aug 16, 2021
Rhino Health Non-Sterile, Powder-free Nitrile Exam Glove
General Hospital
286d