Surgical Principals, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgical Principals, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SPI LaproSac™ Laparoscopic Single-Use Rip-Stop Nylon Specimen Retrieval System, LaproGlide™ Disposable Monopolar PTFE Coated Laparoscopic Probes
2
Total
2
Cleared
0
Denied
Surgical Principals, Inc. has 2 FDA 510(k) cleared medical devices. Based in Pierce, US.
Latest FDA clearance: Sep 2025. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Surgical Principals, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Surgical Principals, Inc.
2 devices