510(k) · Cleared

Cleared

Florida Probe

K875076510(k) TraditionalCleared Mar 10, 198892-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

Florida Probe Corp. · EIX Probe, Periodontic

Cleared on Mar 10, 1988 after a 92-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 2 later devices descend from it.

Decided: Mar 10, 1988
Review: 92 days
Class: Class I
Product code: EIX
Recalls: None
Predicates: 0

2 later devices descend from it, 2 citing it directly.

This deviceK875076 Florida ProbeFlorida Probe Corp. · 1988
Descendant · cites it directly · 0 of its ownK972642 Perio Control IIEstrad B.V. · 1998
Descendant · cites it directly · 0 of its ownK960245 Vip Victor Interactive ProbePro-Dentec · 1996

Most influential descendants

Showing 2 of 2 · See all

K972642Perio Control IIEstrad B.V. · 1998 · cites it directly0descendants
K960245Vip Victor Interactive ProbePro-Dentec · 1996 · cites it directly0descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
0 (this device)	K875076	Florida Probe	Florida Probe Corp.	1988	—
+1	K972642	Perio Control II	Estrad B.V.	1998	—
+1	K960245	Vip Victor Interactive Probe	Pro-Dentec	1996	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
1996	1	0
1998	1	0

FIG. 1 — Lineage of K875076, 1988–1998Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Sources: FDA 510(k) database (decision fields), 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

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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (2)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

Number	Device	Applicant	Decided	Descendants
K972642	Perio Control II	Estrad B.V.	1998	0
K960245	Vip Victor Interactive Probe	Pro-Dentec	1996	0

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, K972642 (Estrad B.V., 1998) has gone furthest, with 0 descendants of its own.

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

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

Year	Median 510(k) review, days	MAUDE reports
2007	—	0
2008	—	0
2009	—	1
2010	—	1
2011	—	1
2012	—	1
2013	—	0
2014	—	0
2015	—	1
2016	—	1
2017	—	0
2018	—	0
2019	—	0
2020	—	0
2021	—	2
2022	—	0
2023	—	0
2024	—	0
2025	—	0
2026	—	—

https://510kreport.com/device/K875076 · printed Nov 6, 2026

Cite this page

510(k) Report. “K875076: Florida Probe.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K875076

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Record history

FDA decision record loaded May 2, 2026
Lineage and recalls computed Nov 3, 2026
Page last updated Nov 3, 2026