Maxxim Medical, Inc. is one of 26006 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Maxxim Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SENICARE ADVANTIX POWDER FREE POLYURETHANE MEDICAL EXAMINATION GLOVE, SENSICARE ADVANTIX POWDER FREE POLYURETHANE DENTAL, EUDERMIC PF POWDER-FREE SURGICAL GLOVES
2
Total
2
Cleared
0
Denied
Maxxim Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Hone Path, US.
Historical record: 2 cleared submissions from 2000 to 2001. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Maxxim Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by N.V. Kema as regulatory consultant.
FDA 510(k) Regulatory Record - Maxxim Medical, Inc.
2 devices