510(k) Report

510(k) · Cleared

Cleared

Encore System

K183310510(k) TraditionalCleared May 9, 2019161-day reviewClass II21 CFR 872.5570

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Siesta Medical, Inc. · ORY Tongue Suspension System

Cleared on May 9, 2019 as substantially equivalent to K133680 (Siesta Medical, Inc., 2014) and 1 other predicate after a 161-day review. Its family tree reaches back 10 generations to 1992. 2 later devices descend from it.

Decided
May 9, 2019
Review
161 days
Class
Class II
Product code
ORY
Recalls
None
Predicates
2

Its longest line of descent runs back 10 generations to K920213 (1992). 18 ancestors in all. 2 later devices descend from it, 1 citing it directly.

  1. Root · 10 generations backK920213 Mitek Anchor, Mitek Anchor IIMitek Surgical Products, Inc. · 1992
  2. 6 generations between
  3. 3 generations backK111179 Encore Tongue Suspension System (Monofilament #1 Suspension Suture)…Siesta Medical, Inc. · 2011
  4. 2 generations backK121440 Encore Tongue Suspension System Encore Removal-Titration KitSiesta Medical, Inc. · 2012
  5. 1 generation backK133680 Encore SystemSiesta Medical, Inc. · 2014
  6. This deviceK183310 Encore SystemSiesta Medical, Inc. · 2019
  7. Descendant · cites it directly · 1 of its ownK201238 Encore SystemSiesta Medical, Inc. · 2020
  8. Descendant · 2 generations on · 0 of its ownK213159 Encore SystemSiesta Medical, Inc. · 2021
Show all 10 generations
  1. Root · 10 generations backK920213 Mitek Anchor, Mitek Anchor IIMitek Surgical Products, Inc. · 1992
  2. 9 generations backK962372 Urotac Bone Anchor InserterInfluence, Inc. · 1996
  3. 8 generations backK970292 IN-Fast Bone Screw System/in-Fast Bone Screw Inserter/in-Fast Bone…Influence, Inc. · 1997 · Recalled
  4. 7 generations backK972023 Sleep-in Bone Screw SystemInfluence, Inc. · 1997
  5. 6 generations backK101060 Siesta Medical, Inc., Prelude Tongue Suspension SystemSiesta Medical, Inc. · 2010
  6. 5 generations backK103179 Prelude II Tounge Suspension SystemSiesta Medical, Inc. · 2010
  7. 4 generations backK110127 Prelude Iii Tongue Suspension SystemSiesta Medical, Inc. · 2011
  8. 3 generations backK111179 Encore Tongue Suspension System (Monofilament #1 Suspension Suture)…Siesta Medical, Inc. · 2011
  9. 2 generations backK121440 Encore Tongue Suspension System Encore Removal-Titration KitSiesta Medical, Inc. · 2012
  10. 1 generation backK133680 Encore SystemSiesta Medical, Inc. · 2014
  11. This deviceK183310 Encore SystemSiesta Medical, Inc. · 2019

Most influential descendants

Showing 2 of 2 · See all
  • K201238Encore SystemSiesta Medical, Inc. · 2020 · cites it directly1descendant
  • K213159Encore SystemSiesta Medical, Inc. · 2021 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−10K920213Mitek Anchor, Mitek Anchor IIMitek Surgical Products, Inc.1992—
−9K962372Urotac Bone Anchor InserterInfluence, Inc.1996—
−8K970292IN-Fast Bone Screw System/in-Fast Bone Screw Inserter/in-Fast Bone ScrewInfluence, Inc.19971
−7K972023Sleep-in Bone Screw SystemInfluence, Inc.1997—
−6K101060Siesta Medical, Inc., Prelude Tongue Suspension SystemSiesta Medical, Inc.2010—
−5K103179Prelude II Tounge Suspension SystemSiesta Medical, Inc.2010—
−4K110127Prelude Iii Tongue Suspension SystemSiesta Medical, Inc.2011—
−3K111179Encore Tongue Suspension System (Monofilament #1 Suspension Suture), Encore…Siesta Medical, Inc.2011—
−2K121440Encore Tongue Suspension System Encore Removal-Titration KitSiesta Medical, Inc.2012—
−1K133680Encore SystemSiesta Medical, Inc.2014—
0 (this device)K183310Encore SystemSiesta Medical, Inc.2019—
+1K201238Encore SystemSiesta Medical, Inc.2020—
+2K213159Encore SystemSiesta Medical, Inc.2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
199530
199620
199910
201310

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
202110
FIG. 1 — Lineage of K183310, 1992–2021Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in ORY? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new ORY device

  1. #1 K201238 Encore Systemscore 6.1 · 11 generations · no Class I recall
  2. #2 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (2)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K133680Encore System
Summary page 4
…snoring and obstructive sleep apnea Device Class Class II Product Code: ORY Predicate Devices Primary: Siesta Medical, Inc., Encore System, K133680 Reference: Medtronic, Inc., AIRvance System, K122391 Device Description The Encore System is designed for anterior tongue base…
Siesta Medical, Inc.2014—
*K122391Medtronic Xomed, Inc.
Summary page 4
…Class Class II Product Code: ORY Predicate Devices Primary: Siesta Medical, Inc., Encore System, K133680 Reference: Medtronic, Inc., AIRvance System, K122391 Device Description The Encore System is designed for anterior tongue base suspension by fixation of the soft tissue of the tongu…
Medtronic Xomed, Inc.2013—

What descends from it? (2)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K201238Encore SystemSiesta Medical, Inc.20201

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 27 years and passes through 3 companies; a new generation was cleared every 1.3 years on median.
  • 3 of the 18 ancestors have a recall of any class.
  • Of its descendants, K201238 (Siesta Medical, Inc., 2020) has gone furthest, with 1 descendant of its own.

How does its category compare?

All ORY devices

ORY Tongue Suspension System: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.

FDA decisions per year · ORY

1in 2021

2010: 22011: 22012: 22014: 12019: 12020: 12021: 1
2007high 2 (2010) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ORY

Too few ORY 510(k)s in any year since 2007 to give a median.

Recalls per year · ORY

No recall names ORY since 2007.

Adverse event reports per year · ORY

5in 2025

2014: 92015: 12018: 22019: 22020: 22022: 22023: 202024: 112025: 5
2007high 20 (2023) · low 0 (2007)2025

MAUDE reports naming product code ORY, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20102—00
20112—00
20122—00
20130—00
20141—09
20150—01
20160—00
20170—00
20180—02
20191—02
20201—02
20211—00
20220—02
20230—020
20240—011
20250—05
20260—0—

What is it indicated for?

The Encore System is intended for anterior advancement of the tongue base and hyoid suspension. It is indicated for the treatment of obstructive sleep apnea (OSA) and / or snoring.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K183310: Encore System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K183310

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026