510(k) Report

510(k) · Cleared

Cleared

Bisco Porcelain Repair Kit

K874557510(k) TraditionalCleared Jan 28, 198885-day reviewClass II21 CFR 872.3765

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

Bisco, Inc. · EBC Sealant, Pit And Fissure, And Conditioner

Cleared on Jan 28, 1988 after an 85-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Jan 28, 1988
Review
85 days
Class
Class II
Product code
EBC
Recalls
None
Predicates
0

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

Descendants, by year cleared 2005: 1 descendant cleared1990200020102020
  1. This deviceK874557 Bisco Porcelain Repair KitBisco, Inc. · 1988
  2. Descendant · cites it directly · 0 of its ownK042804 Tescera Opaquer Powder/Sculpting ResinBisco, Inc. · 2005

Most influential descendants

Showing 1 of 1 · See all
  • K042804Tescera Opaquer Powder/Sculpting ResinBisco, Inc. · 2005 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K874557Bisco Porcelain Repair KitBisco, Inc.1988—
+1K042804Tescera Opaquer Powder/Sculpting ResinBisco, Inc.2005—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200510
FIG. 1 — Lineage of K874557, 1988–2005Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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 EBC? 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 EBC device

  1. #1 K243254 Parkell Pit and Fissure Sealantscore 12.8 · 1 generation · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin 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? (1)

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

NumberDeviceApplicantDecidedDescendants
K042804Tescera Opaquer Powder/Sculpting ResinBisco, Inc.20050

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, K042804 (Bisco, Inc., 2005) has gone furthest, with 0 descendants of its own.

How does its category compare?

All EBC devices

EBC Sealant, Pit And Fissure, And Conditioner: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · EBC

1in 2025

2007: 12008: 12009: 22010: 52011: 32012: 12013: 12014: 12015: 12016: 12017: 22018: 12019: 22023: 22025: 12026 (partial year): 1
2007high 5 (2010) · low 0 (2020)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EBC

80in 2011

2010: 115 days median2011: 80 days median
2007high 115 (2010) · low 80 (2011)2026

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

Recalls per year · EBC

2in 2016

2015: 12016: 2
2007high 2 (2016) · low 0 (2007)2026

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

Adverse event reports per year · EBC

6in 2025

2007: 32008: 12009: 12011: 52013: 112020: 12022: 12023: 22024: 12025: 6
2007high 11 (2013) · low 0 (2010)2025

MAUDE reports naming product code EBC, 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
20071—03
20081—01
20092—01
2010511500
201138005
20121—00
20131—011
20141—00
20151—10
20161—20
20172—00
20181—00
20192—00
20200—01
20210—00
20220—01
20232—02
20240—01
20251—06
20261—0—
Cite this page

510(k) Report. “K874557: Bisco Porcelain Repair Kit.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K874557

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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