510(k) Report

510(k) · Cleared

Cleared

Premier Sealant

K161580510(k) TraditionalCleared Oct 18, 2016132-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

Premier Dental Company Products · EBC Sealant, Pit And Fissure, And Conditioner

Cleared on Oct 18, 2016 after a 132-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 2 later devices descend from it.

Decided
Oct 18, 2016
Review
132 days
Class
Class II
Product code
EBC
Recalls
None
Predicates
0

2 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2025: 1 descendant cleared2026: 1 descendant cleared201620182020202220242026
  1. This deviceK161580 Premier SealantPremier Dental Company Products · 2016
  2. Descendant · cites it directly · 1 of its ownK243254 Parkell Pit and Fissure SealantParkell, Inc. · 2025
  3. Descendant · 2 generations on · 0 of its ownK260819 Any-Com SealMediclus Co., Ltd. · 2026

Most influential descendants

Showing 2 of 2 · See all
  • K243254Parkell Pit and Fissure SealantParkell, Inc. · 2025 · cites it directly1descendant
  • K260819Any-Com SealMediclus Co., Ltd. · 2026 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K161580Premier SealantPremier Dental Company Products2016—
+1K243254Parkell Pit and Fissure SealantParkell, Inc.2025—
+2K260819Any-Com SealMediclus Co., Ltd.2026—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202510
202610
FIG. 1 — Lineage of K161580, 2016–2026Source: 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), the FDA 510(k) statement (indications), 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
Get a 510(k) Report

What was it cleared against?

FDA’s file for it is a 510(k) statement, which names no predicate.

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K243254Parkell Pit and Fissure SealantParkell, Inc.20251

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, K243254 (Parkell, Inc., 2025) has gone furthest, with 1 descendant 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. 2016, this device’s year, is highlighted.

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—

What is it indicated for?

Premier Sealant, a prescription only medical device used for prophylactic sealing of pits and fissures. It may also be used for micro-restorative or “initial layer” of composite restorations.

Indications for use as stated in the FDA 510(k) statement.

Cite this page

510(k) Report. “K161580: Premier Sealant.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K161580

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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