510(k) Report

510(k) · Cleared

Cleared

Hydro-Cast Dental Etching Gel, Model 60025

K990306510(k) TraditionalCleared Mar 3, 199930-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

Kay See Dental Mfg. Co. · EBC Sealant, Pit And Fissure, And Conditioner

Cleared on Mar 3, 1999 as substantially equivalent to K861245 (Ortho Source, 1986) after a 30-day review. Its family tree reaches back 1 generation to 1986.

Decided
Mar 3, 1999
Review
30 days
Class
Class II
Product code
EBC
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K861245 (1986). No later device cites it as a predicate yet.

K861245 · Orthosource Etch Systems · Ortho Source · 19861985199019952000
K861245 · Orthosource Etch Systems · Ortho Source · 19860
  1. Root · 1 generation backK861245 Orthosource Etch SystemsOrtho Source · 1986
  2. This deviceK990306 Hydro-Cast Dental Etching Gel, Model 60025Kay See Dental Mfg. Co. · 1999
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K861245Orthosource Etch SystemsOrtho Source1986—
0 (this device)K990306Hydro-Cast Dental Etching Gel, Model 60025Kay See Dental Mfg. Co.1999—
FIG. 1 — Lineage of K990306, 1986–1999Source: 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
*K861245Orthosource Etch Systems
Summary page 3
…Dental Etching Gel Classification Name - Sealant, Pit, and Fissure, and Conditioner (872.3765) Substantial equivalence claimed to - Orthosource Etch Systems, 872.3765, K861245 Description of the device. The Hydro-Cast Etching Gel is a 35% phosphoric acid solution. It can be applied with a micro-brush, s…
Ortho Source1986—

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?

  • Its one ancestor has no recall.

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?

Hydro-Cast Dental Etching Gel is used to prepare the tooth surface before a dental adhesive is used. It is applied directly on the tooth surface; after fifteen seconds, the tooth surface is rinsed and dried.

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. “K990306: Hydro-Cast Dental Etching Gel, Model 60025.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K990306

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