510(k) Report

510(k) · Cleared

Cleared

Vip Victor Interactive Probe

K960245510(k) TraditionalCleared Apr 4, 199679-day reviewClass I21 CFR 872.4565

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

Pro-Dentec · EIX Probe, Periodontic

Cleared on Apr 4, 1996 as substantially equivalent to K875076 (Florida Probe Corp., 1988) after a 79-day review. Its family tree reaches back 1 generation to 1988.

Decided
Apr 4, 1996
Review
79 days
Class
Class I
Product code
EIX
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K875076 (1988). No later device cites it as a predicate yet.

K875076 · Florida Probe · Florida Probe Corp. · 19881986198819901992199419961998
K875076 · Florida Probe · Florida Probe Corp. · 19880
  1. Root · 1 generation backK875076 Florida ProbeFlorida Probe Corp. · 1988
  2. This deviceK960245 Vip Victor Interactive ProbePro-Dentec · 1996
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K875076Florida ProbeFlorida Probe Corp.1988—
0 (this device)K960245Vip Victor Interactive ProbePro-Dentec1996—
FIG. 1 — Lineage of K960245, 1988–1996Source: 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 EIX? 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? (2)

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
*K875076Florida Probe
Summary page 1
…me of the Device The device is generally known as an Electronic Periodontal Probe. 3. Identification of Predicate Device(s) Florida Probe Corporation’s "Florida Probe,” K875076, and the manual Michigan periodontol probes. 4. Description of the Device The device is a periodontal probe which is used by de…
Florida Probe Corp.1988—
*—manual Michigan periodontol probes
Named without a submission number
—

Also cleared against K875076: 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?

  • Its one ancestor has no recall.
  • 1 other device also cites its predicate K875076.

How does its category compare?

All EIX devices

EIX Probe, Periodontic: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · EIX

FDA has decided no EIX device since 2007.

Median 510(k) review, days · EIX

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

Recalls per year · EIX

No recall names EIX since 2007.

Adverse event reports per year · EIX

2in 2021

2009: 12010: 12011: 12012: 12015: 12016: 12021: 2
2007high 2 (2021) · low 0 (2007)2025

MAUDE reports naming product code EIX, 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—01
20100—01
20110—01
20120—01
20130—00
20140—00
20150—01
20160—01
20170—00
20180—00
20190—00
20200—00
20210—02
20220—00
20230—00
20240—00
20250—00
20260—0—

What is it indicated for?

Pro-Dentec’s VICTOR Interactive Probe is an automated periodontal probe intended for use during periodontal examinations to measure and chart the depth of a gingival sulcus in millimeters.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K960245: Vip Victor Interactive Probe.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K960245

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