510(k) Report

510(k) · Cleared

Cleared

Encore System

K133680510(k) TraditionalCleared Mar 26, 2014114-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 Mar 26, 2014 as substantially equivalent to K121440 (Siesta Medical, Inc., 2012) and 1 other predicate after a 114-day review. Its family tree reaches back 9 generations to 1992. 3 later devices descend from it.

Decided
Mar 26, 2014
Review
114 days
Class
Class II
Product code
ORY
Recalls
None
Predicates
2

Its longest line of descent runs back 9 generations to K920213 (1992). 17 ancestors in all. 3 later devices descend from it, 1 citing it directly.

  1. Root · 9 generations backK920213 Mitek Anchor, Mitek Anchor IIMitek Surgical Products, Inc. · 1992
  2. 5 generations between
  3. 3 generations backK110127 Prelude Iii Tongue Suspension SystemSiesta Medical, Inc. · 2011
  4. 2 generations backK111179 Encore Tongue Suspension System (Monofilament #1 Suspension Suture)…Siesta Medical, Inc. · 2011
  5. 1 generation backK121440 Encore Tongue Suspension System Encore Removal-Titration KitSiesta Medical, Inc. · 2012
  6. This deviceK133680 Encore SystemSiesta Medical, Inc. · 2014
  7. Descendant · cites it directly · 2 of its ownK183310 Encore SystemSiesta Medical, Inc. · 2019
  8. Descendant · 2 generations on · 1 of its ownK201238 Encore SystemSiesta Medical, Inc. · 2020
  9. Descendant · 3 generations on · 0 of its ownK213159 Encore SystemSiesta Medical, Inc. · 2021
Show all 9 generations
  1. Root · 9 generations backK920213 Mitek Anchor, Mitek Anchor IIMitek Surgical Products, Inc. · 1992
  2. 8 generations backK962372 Urotac Bone Anchor InserterInfluence, Inc. · 1996
  3. 7 generations backK970292 IN-Fast Bone Screw System/in-Fast Bone Screw Inserter/in-Fast Bone…Influence, Inc. · 1997 · Recalled
  4. 6 generations backK972023 Sleep-in Bone Screw SystemInfluence, Inc. · 1997
  5. 5 generations backK101060 Siesta Medical, Inc., Prelude Tongue Suspension SystemSiesta Medical, Inc. · 2010
  6. 4 generations backK103179 Prelude II Tounge Suspension SystemSiesta Medical, Inc. · 2010
  7. 3 generations backK110127 Prelude Iii Tongue Suspension SystemSiesta Medical, Inc. · 2011
  8. 2 generations backK111179 Encore Tongue Suspension System (Monofilament #1 Suspension Suture)…Siesta Medical, Inc. · 2011
  9. 1 generation backK121440 Encore Tongue Suspension System Encore Removal-Titration KitSiesta Medical, Inc. · 2012
  10. This deviceK133680 Encore SystemSiesta Medical, Inc. · 2014

Most influential descendants

Showing 3 of 3 · See all
  • K183310Encore SystemSiesta Medical, Inc. · 2019 · cites it directly2descendants
  • K201238Encore SystemSiesta Medical, Inc. · 2020 · 2 generations on1descendant
  • K213159Encore SystemSiesta Medical, Inc. · 2021 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K920213Mitek Anchor, Mitek Anchor IIMitek Surgical Products, Inc.1992—
−8K962372Urotac Bone Anchor InserterInfluence, Inc.1996—
−7K970292IN-Fast Bone Screw System/in-Fast Bone Screw Inserter/in-Fast Bone ScrewInfluence, Inc.19971
−6K972023Sleep-in Bone Screw SystemInfluence, Inc.1997—
−5K101060Siesta Medical, Inc., Prelude Tongue Suspension SystemSiesta Medical, Inc.2010—
−4K103179Prelude II Tounge Suspension SystemSiesta Medical, Inc.2010—
−3K110127Prelude Iii Tongue Suspension SystemSiesta Medical, Inc.2011—
−2K111179Encore Tongue Suspension System (Monofilament #1 Suspension Suture), Encore…Siesta Medical, Inc.2011—
−1K121440Encore Tongue Suspension System Encore Removal-Titration KitSiesta Medical, Inc.2012—
0 (this device)K133680Encore SystemSiesta Medical, Inc.2014—
+1K183310Encore SystemSiesta Medical, Inc.2019—
+2K201238Encore SystemSiesta Medical, Inc.2020—
+3K213159Encore 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
201910
202010
202110
FIG. 1 — Lineage of K133680, 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
*K121440Encore Tongue Suspension System Encore Removal-Titration Kit
Summary page 1
…RY Predicate Device Manufacturer Device Name 510(k) Number Siesta Medical, Inc. ENCORE Tongue K 12 1440 ______________________ -Suspension System Medtronic, Inc. AlRvance System K122…
Siesta Medical, Inc.2012—
*K122391Medtronic Xomed, Inc.
Summary page 1
…ENCORE Tongue K 12 1440 ______________________ -Suspension System Medtronic, Inc. AlRvance System K122391 Device Description The ENCORE System is designed for anterior tongue base suspension by fixation of the soft tissue of the tongue…
Medtronic Xomed, Inc.2013—

What descends from it? (3)

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

NumberDeviceApplicantDecidedDescendants
K183310Encore SystemSiesta Medical, Inc.20192

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 22 years and passes through 3 companies; a new generation was cleared every 8 months on median.
  • 3 of the 17 ancestors have a recall of any class.
  • Of its descendants, K183310 (Siesta Medical, Inc., 2019) has gone furthest, with 2 descendants 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. 2014, 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 to be used for anterior advancement of the tongue base. It is also suitable for performing hyoid suspension. It is indicated for the treatment of mild or moderate obstructive sleep apnea (OSA) and for snoring.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K133680: 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/K133680

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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