510(k) Report

510(k) · Cleared

Cleared

Artas System From Restoration Robotics

K123154510(k) TraditionalCleared Feb 19, 2013133-day reviewClass II21 CFR 882.4560

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

Restoration Robotics, Inc. · ONA Computer Assisted Hair Harvesting System

Cleared on Feb 19, 2013 as substantially equivalent to K103428 (Restoration Robotics, Inc., 2011) after a 133-day review. Its family tree reaches back 8 generations to 1994.

Decided
Feb 19, 2013
Review
133 days
Class
Class II
Product code
ONA
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K930667 (1994). 38 ancestors in all, the oldest K811452 (1981). No later device cites it as a predicate yet.

  1. Root · 8 generations backK930667 Reusable Laparoscopic InstrumentsSnowden-Pencer · 1994 · Recalled
  2. 7 generations backK960400 Diamond-Touch and Micro Diamond-Touch Instruments/Diamond-Line…Snowden-Pencer · 1996
  3. 6 generations backK990144 Intuitive Surgical Endoscopic Instruments, Intuitive Surgical…Intuitive Surgical, Inc. · 2000 · Recalled
  4. 5 generations backK021036 Intuitive Surgical DA Vinci Surgical System, Model IS1000Intuitive Surgical, Inc. · 2002 · Recalled
  5. 4 generations backK040237 Intuitive Surgical DA Vinci Endoscopic Instrument Control System and…Intuitive Surgical, Inc. · 2004
  6. 3 generations backK043153 Intuitive Surgical DA Vinci Surgical System and Endoscopic…Intuitive Surgical, Inc. · 2004
  7. 2 generations backK072629 Digimatch Robodoc Surgical SystemIntegrated Surgical Systems, Inc. · 2008
  8. 1 generation backK103428 The Artas System From Restoration RoboticsRestoration Robotics, Inc. · 2011
  9. This deviceK123154 Artas System From Restoration RoboticsRestoration Robotics, Inc. · 2013
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K930667Reusable Laparoscopic InstrumentsSnowden-Pencer199415
−7K960400Diamond-Touch and Micro Diamond-Touch Instruments/Diamond-Line…Snowden-Pencer1996—
−6K990144Intuitive Surgical Endoscopic Instruments, Intuitive Surgical Endoscopic…Intuitive Surgical, Inc.20003
−5K021036Intuitive Surgical DA Vinci Surgical System, Model IS1000Intuitive Surgical, Inc.200218
−4K040237Intuitive Surgical DA Vinci Endoscopic Instrument Control System and…Intuitive Surgical, Inc.2004—
−3K043153Intuitive Surgical DA Vinci Surgical System and Endoscopic Instruments, Models…Intuitive Surgical, Inc.2004—
−2K072629Digimatch Robodoc Surgical SystemIntegrated Surgical Systems, Inc.2008—
−1K103428The Artas System From Restoration RoboticsRestoration Robotics, Inc.2011—
0 (this device)K123154Artas System From Restoration RoboticsRestoration Robotics, Inc.2013—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198120
198710
198810
199110
199210
199310
199420
199530
199750
199810
199910
200010
200130
200240
200410
200520
FIG. 1 — Lineage of K123154, 1994–2013Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 ONA? 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
Get a 510(k) Report

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
*K103428The Artas System From Restoration Robotics
Summary page 2
…Y Generic/Common Name: Stereotaxic Instrument PREDICATE DEVICES The ARTASTM System is substantially equivalent to the following predicate device: ARTASTM System, K103428 INDICATIONS FOR USE The ARTAS '.System from Restoration Robotics is indicated for harvesting hair follicles from the scalp in m…
Restoration Robotics, Inc.2011—

Also cleared against K103428: 1 other 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.

What does this lineage say?

  • The line of descent spans 19 years and passes through 4 companies; a new generation was cleared every 2.0 years on median.
  • 3 of the 38 ancestors have a recall of any class.
  • 1 other device also cites its predicate K103428.

How does its category compare?

All ONA devices

ONA Computer Assisted Hair Harvesting System: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.

FDA decisions per year · ONA

1in 2018

2011: 12013: 22018: 1
2007high 2 (2013) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ONA

Too few ONA 510(k)s in any year since 2007 to give a median.

Recalls per year · ONA

4in 2013

2013: 4
2007high 4 (2013) · low 0 (2007)2026

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

Adverse event reports per year · ONA

1in 2015

2013: 12015: 1
2007high 1 (2013) · low 0 (2007)2025

MAUDE reports naming product code ONA, 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
20100—00
20111—00
20120—00
20132—41
20140—00
20150—01
20160—00
20170—00
20181—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—

What is it indicated for?

The ARTAS System from Restoration Robotics is indicated for harvesting hair follicles from the scalp in men diagnosed with androgenic alopecia (male pattern hair loss) who have black or brown straight hair. The ARTAS System from Restoration Robotics is intended to assist physicians in identifying and extracting hair follicular units from the scalp during hair transplantation.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K123154: Artas System From Restoration Robotics.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K123154

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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