De Novo · Granted
GrantedAletta® Autonomous Robotic Phlebotomy Device (ARPD™) (Gen1 US)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Vitestro · SIW Robotic Peripheral Venous Blood Collection System
Granted on Aug 19, 2026 as a new device type through De Novo after a 327-day review.
- Decided
- Aug 19, 2026
- Review
- 327 days
- Class
- Class II
- Product code
- SIW
- Recalls
- None
De Novo grants create a new device type without a predicate, so this family tree starts here.
Sources: FDA De Novo 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 SIW? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
Does it have a predicate?
De Novo decisions do not claim a predicate device.
What descends from it?
No later submission names this one as a predicate yet.
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.
How does its category compare?
All SIW devicesSIW Robotic Peripheral Venous Blood Collection System: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, this device’s year, is highlighted.
FDA decisions per year · SIW
1so far in 2026, the most since 2007
2026 to Oct 25, outlined.
Median 510(k) review, days · SIW
Too few SIW 510(k)s in any year since 2007 to give a median.
Recalls per year · SIW
No recall names SIW since 2007.
Adverse event reports per year · SIW
No MAUDE report names SIW since 2007.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
The Aletta® ARPD™ is intended to perform autonomous, ultrasound-guided, venipuncture and
collection of blood for diagnostic purposes in adult outpatients, monitored by a trained phlebotomist.
One phlebotomist may supervise up to three Aletta® ARPD™ devices simultaneously.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/DEN250046 · printed Nov 6, 2026
Cite this page
510(k) Report. “DEN250046: Aletta® Autonomous Robotic Phlebotomy Device (ARPD™) (Gen1 US).” Lineage record from FDA De Novo data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/DEN250046
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Record history
- FDA decision record loaded Oct 30, 2026
- Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
- Page last updated Nov 3, 2026