510(k) · Cleared
ClearedTerason uSmart3200T Ultrasound System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Teratech Corp. · IYN System, Imaging, Pulsed Doppler, Ultrasonic
Cleared on May 9, 2015 as substantially equivalent to K140524 (Teratech Corp., 2014) and 6 other predicates after a 68-day review. Its family tree reaches back 16 generations to 1995. 6 of the 149 devices in its family, counting itself, have a Class I recall. 2 later devices descend from it.
- Decided
- May 9, 2015
- Review
- 68 days
- Class
- Class II
- Product code
- IYN
- Recalls
- None
- Predicates
- 8
Its longest line of descent runs back 16 generations to K935595 (1995). 146 ancestors in all, the oldest K882383 (1988). 2 later devices descend from it, 1 citing it directly. 6 of the 149 devices in this family, counting this one, have a Class I recall.
- Root · 16 generations backK935595 Acuson Model 3001Acuson Corp. · 1995
- 12 generations between
- 3 generations backK112255 AixplorerSupersonic Imagine · 2012
- 2 generations backK130499 IU22 Diagnostic Ultrasound SystemPhilips Ultrasound, Inc. · 2013 · Recalled
- 1 generation backK132304 Epiq Diagnostic Ultrasound SystemPhilips Ultrasound, Inc. · 2013 · Recalled
- This deviceK150533 Terason uSmart3200T Ultrasound SystemTeratech Corp. · 2015
- Descendant · cites it directly · 1 of its ownK193510 Terason uSmart3200T Ultrasound SystemTeratech Corporation · 2020
- Descendant · 2 generations on · 0 of its ownK201633 Terason uSmart 3200T Plus Ultrasound SystemTeratech Corporation · 2020
Show all 16 generations
- Root · 16 generations backK935595 Acuson Model 3001Acuson Corp. · 1995
- 15 generations backK973767 Harmonic Imaging with ContrastAcuson Corp. · 1997
- 14 generations backK022567 Sequoia Signature II Diagnostic Ultrasound SystemAcuson Corp. · 2002
- 13 generations backK032114 Sequoia 8.0 Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2003
- 12 generations backK041319 Sequoia Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2004
- 11 generations backK042770 Modification to Acuson CV70 Cardiovascular SystemSiemens Medical Solutions USA, Inc. · 2004 · Recalled
- 10 generations backK050240 Modification to Acuson CV70 Cardiovascular SystemSiemens Medical Solutions USA, Inc. · 2005 · Recalled
- 9 generations backK052894 Sonoline G60 S Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2005 · Recalled
- 8 generations backK063138 Modification to Acuson Antares Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2006
- 7 generations backK063803 Acuson Antares Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc., Ultrasound DI · 2007 · Recalled
- 6 generations backK072786 Acuson S2000 Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2007
- 5 generations backK091970 Aixplorer Ultrasound SystemSupersonic Imagine · 2009
- 4 generations backK102041 AixplorerSupersonic Imagine · 2010
- 3 generations backK112255 AixplorerSupersonic Imagine · 2012
- 2 generations backK130499 IU22 Diagnostic Ultrasound SystemPhilips Ultrasound, Inc. · 2013 · Recalled
- 1 generation backK132304 Epiq Diagnostic Ultrasound SystemPhilips Ultrasound, Inc. · 2013 · Recalled
- This deviceK150533 Terason uSmart3200T Ultrasound SystemTeratech Corp. · 2015
Class I recalls in this family
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −16 | K935595 | Acuson Model 3001 | Acuson Corp. | 1995 | — |
| −15 | K973767 | Harmonic Imaging with Contrast | Acuson Corp. | 1997 | — |
| −14 | K022567 | Sequoia Signature II Diagnostic Ultrasound System | Acuson Corp. | 2002 | — |
| −13 | K032114 | Sequoia 8.0 Diagnostic Ultrasound System | Siemens Medical Solutions USA, Inc. | 2003 | — |
| −12 | K041319 | Sequoia Diagnostic Ultrasound System | Siemens Medical Solutions USA, Inc. | 2004 | — |
| −11 | K042770 | Modification to Acuson CV70 Cardiovascular System | Siemens Medical Solutions USA, Inc. | 2004 | 1 |
| −10 | K050240 | Modification to Acuson CV70 Cardiovascular System | Siemens Medical Solutions USA, Inc. | 2005 | 1 |
| −9 | K052894 | Sonoline G60 S Ultrasound System | Siemens Medical Solutions USA, Inc. | 2005 | 1 |
| −8 | K063138 | Modification to Acuson Antares Ultrasound System | Siemens Medical Solutions USA, Inc. | 2006 | — |
| −7 | K063803 | Acuson Antares Diagnostic Ultrasound System | Siemens Medical Solutions USA, Inc., Ultrasound DI | 2007 | 9 |
| −6 | K072786 | Acuson S2000 Ultrasound System | Siemens Medical Solutions USA, Inc. | 2007 | — |
| −5 | K091970 | Aixplorer Ultrasound System | Supersonic Imagine | 2009 | — |
| −4 | K102041 | Aixplorer | Supersonic Imagine | 2010 | — |
| −3 | K112255 | Aixplorer | Supersonic Imagine | 2012 | — |
| −2 | K130499 | IU22 Diagnostic Ultrasound System | Philips Ultrasound, Inc. | 2013 | 2 |
| −1 | K132304 | Epiq Diagnostic Ultrasound System | Philips Ultrasound, Inc. | 2013 | 36 |
| 0 (this device) | K150533 | Terason uSmart3200T Ultrasound System | Teratech Corp. | 2015 | — |
| +1 | K193510 | Terason uSmart3200T Ultrasound System | Teratech Corporation | 2020 | — |
| +2 | K201633 | Terason uSmart 3200T Plus Ultrasound System | Teratech Corporation | 2020 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1988 | 1 | 0 |
| 1989 | 1 | 0 |
| 1992 | 1 | 0 |
| 1993 | 1 | 0 |
| 1994 | 5 | 0 |
| 1995 | 5 | 0 |
| 1996 | 3 | 1 |
| 1997 | 7 | 0 |
| 1998 | 10 | 3 |
| 1999 | 11 | 0 |
| 2000 | 12 | 1 |
| 2001 | 12 | 0 |
| 2002 | 14 | 0 |
| 2003 | 11 | 0 |
| 2004 | 13 | 1 |
| 2005 | 8 | 0 |
| 2006 | 3 | 0 |
| 2007 | 2 | 0 |
| 2008 | 2 | 0 |
| 2010 | 1 | 0 |
| 2011 | 2 | 0 |
| 2012 | 2 | 0 |
| 2013 | 1 | 0 |
| 2014 | 2 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2020 | 2 | 0 |
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.
6 devices in this family have a Class I recall. 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 IYN device
- #1 K240850 EPIQ Series Diagnostic Ultrasound Systems…score 32.1 · 24 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (8)
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; numbers the summary cites that cannot be its predicate are marked – and kept off the family tree.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K140524 | Terason USMART3200 and Benq UP200ULTRASOUND SystemSummary page 16…ging System (21 CFR 892.1560, 90-IYO) Diagnostic Ultrasonic Transducer (21 CFR 892.1570, 90-ITX) 3. Predicate Device Terason uSmart3200T Ultrasound System (K140524) Supporting Predicate Devices: Terason™ T3000 8MC3 Transducer (K112953) Philips (Oldelft) S7-3t TE Transducer Probe (K1… | 2014 |
| * | K112953 | Terason T3000 Ultrasound Systems with Updated Needle Guidance GraphicsSummary page 13…of follicle development. h Includes guidance of amniocentesis, infertility monitoring of follicle development. Additional Comments: P1: uses previously cleared under K112953 Prescription Use ___x___ AND/OR Over-The-Counter Use _______ (Part 21 CFR 801 Subpart D)… | 2012 |
| * | K132304 | Epiq Diagnostic Ultrasound SystemSummary page 16…son uSmart3200T Ultrasound System (K140524) Supporting Predicate Devices: Terason™ T3000 8MC3 Transducer (K112953) Philips (Oldelft) S7-3t TE Transducer Probe (K132304) Aloka/Terason Ultrasound System with PDOF Transducer (K110482) Terason uSmart3300 8L2 and 8V3A Transducers (K140773) So… | 2013 |
| * | K070792 | Qlab QuantificationSummary page 21…Philips S7-3t trans-esophageal K132304 (Philips EPIQ) K070792 (Philips iE33) Terason PDOF Aloka UST-T109 PDOF K110482 (Aloka ProSound C3… | 2007 |
| * | K110482 | Prosound C3 / C3 CV Ultrasound SystemsSummary page 16…te Devices: Terason™ T3000 8MC3 Transducer (K112953) Philips (Oldelft) S7-3t TE Transducer Probe (K132304) Aloka/Terason Ultrasound System with PDOF Transducer (K110482) Terason uSmart3300 8L2 and 8V3A Transducers (K140773) Sonosite Edge System L25x/13-6 Transducer (K082098)… | 2011 |
| * | K140773 | Terason USMART3300 Ultrasound SystemSummary page 4…ng of follicle development. h Includes guidance of amniocentesis, infertility monitoring of follicle development. Additional Comments: P1: uses previously cleared under K140773 Prescription Use ___x___ AND/OR Over-The-Counter Use _______ (Part 21 CFR 801 Subpart D)… | 2014 |
| * | K082098 | Sonosite Maxx Series Ultrasound SystemSummary page 16…Aloka/Terason Ultrasound System with PDOF Transducer (K110482) Terason uSmart3300 8L2 and 8V3A Transducers (K140773) Sonosite Edge System L25x/13-6 Transducer (K082098) 4. Intended Use The Teratech Corporation Terason™ uSmart3200T is a general purpose Ultrasound System inten… | 2008 |
| Kept off the family tree | K071792 | Sonosite Maxx Not in FDA’s 510(k), De Novo or PMA lists as we hold them (a misreading, a typo, or a number FDA does not list), so it is kept off the family tree Summary page 19…ssion) K140524 Sonosite Maxx K071792 Intended Use Diagnostic Ultrasound Diagnostic Ultrasound Diagnostic Ultrasound… |
What descends from it? (2)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K193510 | Terason uSmart3200T Ultrasound System | 2020 | 1 |
Has anything in its family been recalled? (6 Class I)
No FDA recall names this device.
Relatives with a Class I recall
Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.
- K040050Instatrak System with Multiple Dataset Navigation, Model IT3500Ge Medical Systems Navigation and Visualization IN · 2004 · 4 generations back · ◆ in the 2004 ancestors bar of FIG. 11 Class I recall
- K994270Instatrak 3000 System with Fluorotrak Module, Model IT3000Visualization Technology, Inc. · 2000 · 4 generations back · ◆ in the 2000 ancestors bar of FIG. 12 Class I recalls
- K983529Instatrak 3000Visualization Technology, Inc. · 1998 · 4 generations back · ◆ in the 1998 ancestors bar of FIG. 11 Class I recall
- K982994Skull Base Instatrak SystemVisualization Technology, Inc. · 1998 · 4 generations back · ◆ in the 1998 ancestors bar of FIG. 11 Class I recall
- K981998Pediatric Instatrak SystemVisualization Technology, Inc. · 1998 · 4 generations back · ◆ in the 1998 ancestors bar of FIG. 11 Class I recall
- K960330InstatrakVisualization Technology, Inc. · 1996 · 4 generations back · ◆ in the 1996 ancestors bar of FIG. 11 Class I recall
Nearest 5 of 6; all are on the web page.
What does this lineage say?
- The line of descent spans 20 years and passes through 6 companies; a new generation was cleared every 11 months on median.
- 45 of the 146 ancestors have a recall of any class; 6 have a Class I recall.
- Of its descendants, K193510 (Teratech Corporation, 2020) has gone furthest, with 1 descendant of its own.
How does its category compare?
All IYN devicesIYN System, Imaging, Pulsed Doppler, Ultrasonic: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.
FDA decisions per year · IYN
57in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · IYN
124in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · IYN
10in 2025
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · IYN
610in 2025
MAUDE reports naming product code IYN, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 13 | 26 | 16 | 3 |
| 2008 | 25 | 18 | 12 | 2 |
| 2009 | 18 | 29 | 8 | 9 |
| 2010 | 29 | 67 | 10 | 17 |
| 2011 | 39 | 46 | 8 | 18 |
| 2012 | 43 | 37 | 3 | 20 |
| 2013 | 51 | 60 | 8 | 18 |
| 2014 | 56 | 39 | 2 | 48 |
| 2015 | 54 | 55 | 3 | 116 |
| 2016 | 60 | 56 | 2 | 145 |
| 2017 | 64 | 83 | 0 | 146 |
| 2018 | 59 | 85 | 7 | 85 |
| 2019 | 47 | 79 | 0 | 59 |
| 2020 | 57 | 72 | 4 | 67 |
| 2021 | 46 | 105 | 8 | 213 |
| 2022 | 53 | 105 | 10 | 186 |
| 2023 | 44 | 115 | 4 | 229 |
| 2024 | 50 | 119 | 1 | 266 |
| 2025 | 57 | 124 | 10 | 610 |
| 2026 | 44 | 107 | 2 (1) | — |
What is it indicated for?
The Teratech Corporation Terason™ uSmart3200T is a general purpose Ultrasound System intended for use by a qualified physician for evaluation by ultrasound imaging or fluid flow analysis of the human body. Specific clinical applications and exam types include: Ophthalmic, Fetal, Abdominal, Intra-operative (Spec. and Neuro.), Pediatrics, Small Organ (Thyroid, Breast, Testes); Neonatal and Adult Cephalic, Trans-rectal, Trans-vaginal, Trans-esophageal (non-cardiac), Musculo-skeletal (Conventional and Superficial), Cardiac (Adult & Pediatric), Trans-esophageal (cardiac), and Peripheral Vascular.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K150533 · printed Nov 6, 2026
Cite this page
510(k) Report. “K150533: Terason uSmart3200T Ultrasound System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K150533
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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