510(k) · Cleared

Cleared

PRO-V

K073263510(k) TraditionalCleared Feb 14, 200886-day reviewClass II21 CFR 872.3770

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

Bisco, Inc. · EBG Crown And Bridge, Temporary, Resin

Cleared on Feb 14, 2008 as substantially equivalent to K924132 (Cosmedent, Inc., 1993) after an 86-day review. Its family tree reaches back 1 generation to 1993. 1 later device descends from it.

Decided: Feb 14, 2008
Review: 86 days
Class: Class II
Product code: EBG
Recalls: None
Predicates: 1

Its longest line of descent runs back 1 generation to K924132 (1993). 1 later device descends from it, 1 citing it directly.

By dateBy generation

Root · 1 generation backK924132 E.Z. Temep, Temporary Filling MaterialCosmedent, Inc. · 1993
This deviceK073263 PRO-VBisco, Inc. · 2008
Descendant · cites it directly · 0 of its ownK103514 Pro-V CoatBisco, Inc. · 2011

Most influential descendants

Showing 1 of 1 · See all

K103514Pro-V CoatBisco, Inc. · 2011 · cites it directly0descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−1	K924132	E.Z. Temep, Temporary Filling Material	Cosmedent, Inc.	1993	—
0 (this device)	K073263	PRO-V	Bisco, Inc.	2008	—
+1	K103514	Pro-V Coat	Bisco, Inc.	2011	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2011	1	0

FIG. 1 — Lineage of K073263, 1993–2011Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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 EBG? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new EBG device

#1 K253380 “FLNT Base” and “FLNT Temp”score 12.4 · 6 generations · no Class I recall
#2 Held for the reportin the report
#3 Held for the reportin the report

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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.

Type	Number	Device	Applicant	Decided	Recalls
*	K924132	E.Z. Temep, Temporary Filling Material Summary page 1 …LL. can then be easily removed when no longler needed anid tile PRO-V COAT is simply rnosed off vith copious amounts of water. Prcdicate Devices: £4-Temp cleared under (K9241 32) dated July 8, 1993. Significant Performance Characteristics: SUBSTANTIAL EQUJE 'VALENCE SUMMARY…	Cosmedent, Inc.	1993	—

What descends from it? (1)

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

Number	Device	Applicant	Decided	Descendants
K103514	Pro-V Coat	Bisco, Inc.	2011	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?

Its one ancestor has no recall.
Of its descendants, K103514 (Bisco, Inc., 2011) has gone furthest, with 0 descendants of its own.

How does its category compare?

All EBG devices

EBG Crown And Bridge, Temporary, Resin: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

FDA decisions per year · EBG

4in 2025

2007high 14 (2020) · low 2 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EBG

106in 2025

2007high 265 (2021) · low 64 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · EBG

1in 2020

2007high 1 (2009) · low 0 (2007)2026

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

Adverse event reports per year · EBG

1in 2025

2007high 26 (2015) · low 0 (2018)2025

MAUDE reports naming product code EBG, not matched to any one device; reports are not rates.

View these four charts as a table

Year	Decisions	Median 510(k) review, days	Recalls (Class I)	MAUDE reports
2007	3	64	0	4
2008	9	83	0	4
2009	2	—	1	1
2010	5	103	0	1
2011	10	96	0	1
2012	5	90	0	5
2013	2	—	0	11
2014	3	114	0	23
2015	6	209	0	26
2016	4	163	0	8
2017	2	—	0	4
2018	4	202	0	0
2019	6	98	0	6
2020	14	194	1	2
2021	3	265	0	4
2022	3	73	0	2
2023	2	—	0	0
2024	5	144	0	0
2025	4	106	0	1
2026	2	—	0	—

What is it indicated for?

PRO-V is a line of provisional restorative materials designed to address the differing requirements for creating or placing any provisional restoration. The PRO-V System consists of PRO-V FLO, PRO-V FILL, and PRO-V COAT which offers a complete solution to create an effective inlay or onlay provisional.

Indications for Use:

A. Temporary fillings

B. Provisional Inlays

C. Provisional Onlays

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K073263 · printed Nov 6, 2026

Cite this page

510(k) Report. “K073263: PRO-V.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K073263

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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