Anexa Biomedical, Inc. is one of 18376 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Anexa Biomedical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Anexa Wound Flush, USP Sterile Water, and USP Sterile Normal Saline (0.9% sodium chloride) 120 mL cup, USP Sterile Water, and USP Sterile Normal Saline (0.9% sodium chloride) 100mL bottle, USP Sterile Water, and USP Sterile Normal Saline (0.9% sodium chloride) 250mL bottle, USP Sterile Water, and USP Sterile Normal Saline (0.9% sodium chloride) 500mL bottle, Anexa Wound Flush, Sterile Water & Sterile Normal Saline
2
Total
2
Cleared
0
Denied
Anexa Biomedical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Zephyrhills, US.
Historical record: 2 cleared submissions from 2016 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Anexa Biomedical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Smith Assoicates as regulatory consultant.
FDA 510(k) Regulatory Record - Anexa Biomedical, Inc.
2 devices