510(k) Report

510(k) · Cleared

Cleared

Ultrasonic Biometer/Pachymeter for Opthalmology Odm 2100 and Odm 2200

K063433510(k) TraditionalCleared Jan 29, 200777-day reviewClass II21 CFR 892.1560

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

Meda, Ltd. · IYO System, Imaging, Pulsed Echo, Ultrasonic

Cleared on Jan 29, 2007 as substantially equivalent to K040668 (Sonomed, Inc., 2004) after a 77-day review. Its family tree reaches back 2 generations to 1985. 1 later device descends from it.

Decided
Jan 29, 2007
Review
77 days
Class
Class II
Product code
IYO
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K843696 (1985). 3 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1985: 1 other ancestor2023: 1 descendant clearedK843696 · Ophthalmic a-Scan a-2000 Sonome · Sonomed Technology, Inc. · 1985K040668 · E-Z Scan AB5500+ · Sonomed, Inc. · 20041990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor 1 generation forward: 1 descendant K040668 · E-Z Scan AB5500+ · Sonomed, Inc. · 2004K843696 · Ophthalmic a-Scan a-2000 Sonome · Sonomed Technology, Inc. · 19850
  1. Root · 2 generations backK843696 Ophthalmic a-Scan a-2000 SonomeSonomed Technology, Inc. · 1985
  2. 1 generation backK040668 E-Z Scan AB5500+Sonomed, Inc. · 2004
  3. This deviceK063433 Ultrasonic Biometer/Pachymeter for Opthalmology Odm 2100 and Odm 2200Meda, Ltd. · 2007
  4. Descendant · cites it directly · 0 of its ownK222787 Sunkingdom Ophthalmic Ultrasound Examination Instrument SK-3000A…Chongqing Sunkingdom Medical Instrument Co., Ltd. · 2023

Most influential descendants

Showing 1 of 1 · See all
  • K222787Sunkingdom Ophthalmic Ultrasound Examination Instrument SK-3000A, SK-3000B, SK-3000C…Chongqing Sunkingdom Medical Instrument Co., Ltd. · 2023 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K843696Ophthalmic a-Scan a-2000 SonomeSonomed Technology, Inc.1985—
−1K040668E-Z Scan AB5500+Sonomed, Inc.2004—
0 (this device)K063433Ultrasonic Biometer/Pachymeter for Opthalmology Odm 2100 and Odm 2200Meda, Ltd.2007—
+1K222787Sunkingdom Ophthalmic Ultrasound Examination Instrument SK-3000A, SK-3000B…Chongqing Sunkingdom Medical Instrument Co., Ltd.2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198510

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202310
FIG. 1 — Lineage of K063433, 1985–2023Source: 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 IYO? 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 IYO device

  1. #1 K243937 Accuro 3Sscore 20.5 · 18 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
*K040668E-Z Scan AB5500+
Summary page 1
…fication Name: Ultrasonic Pulsed Echo Imaging System Regulation Number: 892.1560 Product Code: 90-IYO 3) Predicate Devices Sonomned Medical E-Z ScanTM AB5500, K040668 4) Intended Use The intended use of the ODM-2100 & ODM-2200 includes the location and visualization of ophthalmic disorde…
Sonomed, Inc.2004—

Also cleared against K040668: 3 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K222787Sunkingdom Ophthalmic Ultrasound Examination Instrument SK-3000A, SK-3000B, SK-3000C…Chongqing Sunkingdom Medical Instrument Co., Ltd.20230

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 19.1 years on median.
  • None of the 3 ancestors has a recall.
  • Of its descendants, K222787 (Chongqing Sunkingdom Medical Instrument Co., Ltd., 2023) has gone furthest, with 0 descendants of its own.
  • 3 other devices also cite its predicate K040668.

How does its category compare?

All IYO devices

IYO System, Imaging, Pulsed Echo, Ultrasonic: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.

FDA decisions per year · IYO

7in 2025

2007: 202008: 142009: 132010: 152011: 112012: 152013: 172014: 142015: 192016: 102017: 192018: 142019: 132020: 112021: 152022: 52023: 112024: 102025: 72026 (partial year): 10
2007high 20 (2007) · low 5 (2022)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · IYO

171in 2025

2007: 17 days median2008: 36 days median2009: 79 days median2010: 113 days median2011: 69 days median2012: 68 days median2013: 50 days median2014: 63 days median2015: 46 days median2016: 36 days median2017: 72 days median2018: 56 days median2019: 59 days median2020: 57 days median2021: 64 days median2022: 190 days median2023: 177 days median2024: 220 days median2025: 171 days median2026 (partial year): 139 days median
2007high 220 (2024) · low 17 (2007)2026

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

Recalls per year · IYO

1in 2022

2007: 42008: 52009: 92010: 82012: 22013: 32014: 22015: 12018: 12019: 12021: 112022: 12026 (partial year): 1
2007high 11 (2021) · low 0 (2011)2026

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

Adverse event reports per year · IYO

485in 2025

2007: 392008: 202009: 272010: 202011: 582012: 782013: 4362014: 3042015: 2682016: 2542017: 2382018: 3682019: 5372020: 4982021: 6172022: 5112023: 5272024: 6402025: 485
2007high 640 (2024) · low 20 (2008)2025

MAUDE reports naming product code IYO, 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
20072017439
20081436520
20091379927
201015113820
20111169058
20121568278
201317503436
201414632304
201519461268
201610360254
201719720238
201814561368
201913591537
202011570498
2021156411617
202251901511
2023111770527
2024102200640
202571710485
2026101391—

What is it indicated for?

• Ultrasound Imaging of the eye

• Axial biometric parameter measurement of the eye

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K063433: Ultrasonic Biometer/Pachymeter for Opthalmology Odm 2100 and Odm 2200.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K063433

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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