510(k) Report

510(k) · Cleared

Cleared

Hummingbird (TM) Tympanostomy Tube System (TTS)

K142282510(k) TraditionalCleared Apr 23, 2015251-day reviewClass II21 CFR 874.3880

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

Preceptis Medical · ETD Tube, Tympanostomy

Cleared on Apr 23, 2015 as substantially equivalent to K133921 (Preceptis Medical, 2014) after a 251-day review. Its family tree reaches back 3 generations to 1997. 5 later devices descend from it.

Decided
Apr 23, 2015
Review
251 days
Class
Class II
Product code
ETD
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K973226 (1997). 5 later devices descend from it, 1 citing it directly.

  1. Root · 3 generations backK973226 Tubingen Tympanic Ventilation Tube, Tympanic Ventilation Tubes with…Heinz Kurz GmbH Medizintechnik · 1997
  2. 2 generations backK071150 Trocar Ventilation Tube/with Trocar Tip, Trocar Handle, Model 1015…Heinz Kurz GmbH Medizintechnik · 2007
  3. 1 generation backK133921 Preceptis Tympanostomy Tube InserterPreceptis Medical · 2014
  4. This deviceK142282 Hummingbird (TM) Tympanostomy Tube System (TTS)Preceptis Medical · 2015
  5. Descendant · cites it directly · 4 of its ownK200952 Hummingbird Tympanostomy Tube SystemPreceptis Medical, Inc. · 2020
  6. Descendant · 2 generations on · 2 of its ownK221254 Hummingbird Tympanostomy Tube SystemPreceptis Medical, Inc. · 2022
  7. Descendant · 2 generations on · 1 of its ownK232702 Solo+ Tympanostomy Tube Device (TTD)Aventamed Dac · 2024
  8. Descendant · 3 generations on · 0 of its ownK252436 Tula Tympanostomy Tube Delivery DeviceTusker Medical, Inc. · 2026
  9. Descendant · 3 generations on · 0 of its ownK250256 Solo+ Tympanostomy Tube Device (TTD), Solo+ TTD, Solo+ (Solo+…Aventamed Dac · 2025

Most influential descendants

Showing 5 of 5 · See all
  • K200952Hummingbird Tympanostomy Tube SystemPreceptis Medical, Inc. · 2020 · cites it directly4descendants
  • K221254Hummingbird Tympanostomy Tube SystemPreceptis Medical, Inc. · 2022 · 2 generations on2descendants
  • K232702Solo+ Tympanostomy Tube Device (TTD)Aventamed Dac · 2024 · 2 generations on1descendant
  • K252436Tula Tympanostomy Tube Delivery DeviceTusker Medical, Inc. · 2026 · 3 generations on0descendants
  • K250256Solo+ Tympanostomy Tube Device (TTD), Solo+ TTD, Solo+ (Solo+ Tympanostomy Tube…Aventamed Dac · 2025 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K973226Tubingen Tympanic Ventilation Tube, Tympanic Ventilation Tubes with Ene/S…Heinz Kurz GmbH Medizintechnik1997—
−2K071150Trocar Ventilation Tube/with Trocar Tip, Trocar Handle, Model 1015 074, 1015…Heinz Kurz GmbH Medizintechnik2007—
−1K133921Preceptis Tympanostomy Tube InserterPreceptis Medical2014—
0 (this device)K142282Hummingbird (TM) Tympanostomy Tube System (TTS)Preceptis Medical2015—
+1K200952Hummingbird Tympanostomy Tube SystemPreceptis Medical, Inc.2020—
+2K221254Hummingbird Tympanostomy Tube SystemPreceptis Medical, Inc.2022—
+2K232702Solo+ Tympanostomy Tube Device (TTD)Aventamed Dac2024—
+3K252436Tula Tympanostomy Tube Delivery DeviceTusker Medical, Inc.2026—
+3K250256Solo+ Tympanostomy Tube Device (TTD), Solo+ TTD, Solo+ (Solo+ Tympanostomy…Aventamed Dac2025—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
202210
202410
202510
202610
FIG. 1 — Lineage of K142282, 1997–2026Source: 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 ETD? 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 ETD device

  1. #1 K252436 Tula Tympanostomy Tube Delivery Devicescore 12.7 · 6 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

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
*K133921Preceptis Tympanostomy Tube Inserter
Cleared while this submission was under review
Summary page 4
…TTS) Product Code ETD (21 CFR Part 874.3880) Common Tympanostomy Tube Inserter with pre-loaded ventilation tube Name Predicate Preceptis Tympanostomy Tube System, 510(k) K133921 Devices 510(k) Summary — K142282 Device Description The Hummingbird™ Tympanostomy Tube System (TTS) which incl…
Preceptis Medical2014—

What descends from it? (5)

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

NumberDeviceApplicantDecidedDescendants
K200952Hummingbird Tympanostomy Tube SystemPreceptis Medical, Inc.20204

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 18 years and passes through 2 companies; a new generation was cleared every 6.7 years on median.
  • None of the 3 ancestors has a recall.
  • Of its descendants, K200952 (Preceptis Medical, Inc., 2020) has gone furthest, with 4 descendants of its own.

How does its category compare?

All ETD devices

ETD Tube, Tympanostomy: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.

FDA decisions per year · ETD

1in 2025

2007: 22008: 12011: 12014: 12015: 32017: 12020: 12022: 12023: 12024: 22025: 12026 (partial year): 1
2007high 3 (2015) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ETD

92in 2015

2015: 92 days median
2007high 92 (2015)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · ETD

9in 2024

2010: 22012: 12023: 12024: 9
2007high 9 (2024) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · ETD

1in 2025

2007: 12009: 12010: 42011: 12013: 72014: 42015: 42016: 22017: 72018: 22019: 182020: 32021: 82022: 12023: 42024: 22025: 1
2007high 18 (2019) · low 0 (2008)2025

MAUDE reports naming product code ETD, 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
20072—01
20081—00
20090—01
20100—24
20111—01
20120—10
20130—07
20141—04
201539204
20160—02
20171—07
20180—02
20190—018
20201—03
20210—08
20221—01
20231—14
20242—92
20251—01
20261—0—

What is it indicated for?

The Hummingbird™ Tympanostomy Tube System is intended to deliver a tympanostomy tube in tympanostomy procedures

in which the patient is receiving a tympanostomy tube.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K142282: Hummingbird (TM) Tympanostomy Tube System (TTS).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K142282

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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