510(k) Report

510(k) · Cleared

Cleared

Prime & Bond NT Dual Cure Universal Dental Adhesive System

K992518510(k) TraditionalCleared Sep 22, 199956-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

Dentsply Intl. · EBC Sealant, Pit And Fissure, And Conditioner

Cleared on Sep 22, 1999 as substantially equivalent to K982394 (Dentsply Intl., 1998) after a 56-day review. Its family tree reaches back 5 generations to 1993.

Decided
Sep 22, 1999
Review
56 days
Class
Class II
Product code
EBC
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K931812 (1993). 8 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 5 generations backK931812 New Dentine AdhesiveDentsply Intl. · 1993
  2. 4 generations backK960823 Prime & Bond 2.0 Multipurpose Dentin/Enamel Bonding AgentDentsply Intl. · 1996
  3. 3 generations backK962348 Prime & Bond 2.1 Multipurpose Dentin/Enamel Bonding AgentDentsply Intl. · 1996
  4. 2 generations backK964525 Prime & Bond 2.1 M.P. Dentin/Enamel Bonding Agent W/ActivatorDentsply Intl. · 1997
  5. 1 generation backK982394 Prime & Bond NT Dual Cure Universal Dental Adhesive SystemDentsply Intl. · 1998
  6. This deviceK992518 Prime & Bond NT Dual Cure Universal Dental Adhesive SystemDentsply Intl. · 1999
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K931812New Dentine AdhesiveDentsply Intl.1993—
−4K960823Prime & Bond 2.0 Multipurpose Dentin/Enamel Bonding AgentDentsply Intl.1996—
−3K962348Prime & Bond 2.1 Multipurpose Dentin/Enamel Bonding AgentDentsply Intl.1996—
−2K964525Prime & Bond 2.1 M.P. Dentin/Enamel Bonding Agent W/ActivatorDentsply Intl.1997—
−1K982394Prime & Bond NT Dual Cure Universal Dental Adhesive SystemDentsply Intl.1998—
0 (this device)K992518Prime & Bond NT Dual Cure Universal Dental Adhesive SystemDentsply Intl.1999—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199420
199510
FIG. 1 — Lineage of K992518, 1993–1999Source: 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 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? (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.

TypeNumberDeviceApplicantDecidedRecalls
*K982394Prime & Bond NT Dual Cure Universal Dental Adhesive System
Summary page 1
…ME: PRIME & BOND® NT™ DENTAL ADHESIVE SYSTEM CLASSIFICATION NAME: Resin tooth bonding agent 872.3200 PREDICATE DEVICE: Prime & Bond® NT™ Universal Dental Adhesive System K982394 DEVICE DESCRIPTION: PRIME & BOND® NT™ DENTAL ADHESIVE SYSTEM is a one- component, no-mix visible light-curable dental bonding ag…
Dentsply Intl.1998—

Also cleared against K982394: 7 other devices →

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?

  • The line of descent spans 6 years and passes through 1 company; a new generation was cleared every 1.0 years on median.
  • None of the 8 ancestors has a recall.
  • 7 other devices also cite its predicate K982394.

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—

What is it indicated for?

Addition of New Indication: To be used in conjunction with pit and fissure sealant

Current Indications, K982394:

Direct composite and compomer restorations

Composite, ceramic and amalgam repairs

Cavity vamish for use with fresh amalgam

Indirect restorations: Dual Cure, inlays, onlays, veneers, crowns and bridges

Endaodontic post cementation

Adhesive bonding of direct amalgam restorations

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. “K992518: Prime & Bond NT Dual Cure Universal Dental Adhesive System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K992518

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