FDA 510(k) Applications for Medical Device Product Code "ORY"
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K183310 | Siesta Medical, Inc | Encore System | 05/09/2019 |
| K133680 | SIESTA MEDICAL, INC. | ENCORE SYSTEM | 03/26/2014 |
| K213159 | Siesta Medical, Inc. | Encore System | 12/22/2021 |
| K201238 | Siesta Medical, Inc. | Encore System | 10/02/2020 |
| K121814 | SIESTA MEDICAL, INC. | ENCORE TONGUE SUSPENSION SYSTEM | 11/07/2012 |
| K111179 | SIESTA MEDICAL, INC. | ENCORE TONGUE SUSPENSION SYSTEM (MONOFILAMENT #1 SUSPENSION SUTURE), ENCORE TONGUE SUSPENSION SYSTEM SYSTEM (MONOFILAMEN | 07/01/2011 |
| K121440 | SIESTA MEDICAL, INC. | ENCORE TONGUE SUSPENSION SYSTEM ENCORE REMOVAL-TITRATION KIT | 12/06/2012 |
| K103179 | SIESTA MEDICAL, INC. | PRELUDE II TOUNGE SUSPENSION SYSTEM | 12/20/2010 |
| K110127 | SIESTA MEDICAL, INC. | PRELUDE III TONGUE SUSPENSION SYSTEM | 04/08/2011 |
| K101060 | SIESTA MEDICAL, INC. | SIESTA MEDICAL, INC., PRELUDE TONGUE SUSPENSION SYSTEM | 07/08/2010 |
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