Siesta Medical, Inc.
Siesta Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2021.
Top product codes for Siesta Medical, Inc.
Recent clearances by Siesta Medical, Inc.
- K213159 — Encore System
- K201238 — Encore System
- K183310 — Encore System
- K133680 — ENCORE SYSTEM
- K121440 — ENCORE TONGUE SUSPENSION SYSTEM ENCORE REMOVAL-TITRATION KIT
- K121814 — ENCORE TONGUE SUSPENSION SYSTEM
- K111179 — ENCORE TONGUE SUSPENSION SYSTEM (MONOFILAMENT #1 SUSPENSION SUTURE), ENCORE TONGUE SUSPENSION SYSTEM SYSTEM (MONOFILAMEN
- K110127 — PRELUDE III TONGUE SUSPENSION SYSTEM
- K103179 — PRELUDE II TOUNGE SUSPENSION SYSTEM
- K101060 — SIESTA MEDICAL, INC., PRELUDE TONGUE SUSPENSION SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.