Transenterix, Inc.
FDA 510(k) medical device clearances.
Top product codes for Transenterix, Inc.
Recent clearances by Transenterix, Inc.
- K202166 — Senhance Surgical System
- K200049 — Senhance Surgical System
- K192877 — Senhance Surgical System
- K191482 — Senhance Surgical System
- K182421 — Senhance Ultrasonic System
- K183098 — Senhance Surgical System
- K181517 — Senhance Surgical System
- K180163 — TransEnterix Senhance Surgical System
- K171120 — Senhance Surgical Robotic System
- K122299 — SPIDER SURGICAL INSTRUMENTS, FLEXIBLE MONOPOLAR GRASPER WAVY RATCHETED, SPIDER SURGICAL INSTRUMENTS, FLEXIBLE MONOPOLAR
- K120403 — SPIDER FLEXIBLE BLUNT DISSECTOR AND BAND PASSER
- K102839 — SPIDER STANDARD AND ADVANCED
- K102646 — SPIDER FLEX MONOPOLAR HOOK
- K091697 — SPIDER SURGICAL INSTRUMENTS, MODELS 90004, 90005, 90007, 90009, 90010, 90012, 90013, 90015
- K090902 — SPIDER SINGLE PORT SURGICAL DEVICE, SUPPORT ARM ACCESSORY, MODEL 90001, 90002, 90003
Data sourced from openFDA. This site is unofficial and independent of the FDA.