Azur Medical Company, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Azur Medical Company, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Medical Surgical Mask, Sterile Auto-Disable Syringes with/without Needle for Single Use, Sterile Hypodermic Needles for Single Use
4
Total
4
Cleared
0
Denied
Azur Medical Company, Inc. has 4 FDA 510(k) cleared medical devices. Based in Richmond, US.
Latest FDA clearance: Mar 2024. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Azur Medical Company, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shanghai Lingfu Technology Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Azur Medical Company, Inc.
4 devices
Cleared
Mar 19, 2024
Medical Surgical Mask
General Hospital
280d
Cleared
Jan 27, 2022
Sterile Auto-Disable Syringes with/without Needle for Single Use
General Hospital
279d
Cleared
Oct 14, 2021
Sterile Hypodermic Needles for Single Use
General Hospital
174d
Cleared
Oct 07, 2021
Sterile syringes for single use with/without needle
General Hospital
167d