510(k) Report

De Novo · Granted

Granted

Brainport V100 Device

DEN130039De NovoGranted Jun 18, 2015680-day reviewClass II21 CFR 886.5905

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

Wicab, Inc. · PIC Oral Electronic Vision Aid

Granted on Jun 18, 2015 as a new device type through De Novo after a 680-day review. 1 later device descends from it.

Decided
Jun 18, 2015
Review
680 days
Class
Class II
Product code
PIC
Recalls
None

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2015: 1 descendant cleared201620182020202220242026
  1. This deviceDEN130039 Brainport V100 DeviceWicab, Inc. · 2015
  2. Descendant · cites it directly · 0 of its ownK152851 BrainPort V100Wicab, Inc. · 2015

Most influential descendants

Showing 1 of 1 · See all
  • K152851BrainPort V100Wicab, Inc. · 2015 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)DEN130039Brainport V100 DeviceWicab, Inc.2015—
+1K152851BrainPort V100Wicab, Inc.2015—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201510
FIG. 1 — Lineage of DEN130039, 2015–2015Source: 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 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 PIC? 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

Does it have a predicate?

De Novo decisions do not claim a predicate device.

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K152851BrainPort V100Wicab, Inc.20150

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?

  • Of its descendants, K152851 (Wicab, Inc., 2015) has gone furthest, with 0 descendants of its own.

How does its category compare?

All PIC devices

PIC Oral Electronic Vision Aid: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.

FDA decisions per year · PIC

2in 2015

2015: 2
2007high 2 (2015) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PIC

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

Recalls per year · PIC

1in 2019

2019: 1
2007high 1 (2019) · low 0 (2007)2026

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

Adverse event reports per year · PIC

No MAUDE report names PIC since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20152—00
20160—00
20170—00
20180—00
20190—10
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—

What is it indicated for?

The BrainPort V100, a prescription device under 21 CFR Part 801.109 that is indicated for use as an oral electronic vision aid that provides electro-tactile stimulation to aid profoundly blind patients in orientation, mobility, and object recognition as an adjunctive device to other assistive methods such as the white cane or a guide dog.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “DEN130039: Brainport V100 Device.” Lineage record from FDA De Novo data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/DEN130039

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