510(k) Report

510(k) · Cleared

Cleared

NOBILCAM IMPAK Disc

K251252510(k) TraditionalCleared Aug 1, 2025100-day reviewClass U

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

Shandong Huge Dental Material Corporation · MQC Mouthguard, Prescription

Cleared on Aug 1, 2025 as substantially equivalent to K111828 (Astron Dental Corporation, 2011) after a 100-day review. Its family tree reaches back 1 generation to 2011.

Decided
Aug 1, 2025
Review
100 days
Class
Class U
Product code
MQC
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K111828 (2011). No later device cites it as a predicate yet.

K111828 · Clearsplint ES · Astron Dental Corporation · 20110
  1. Root · 1 generation backK111828 Clearsplint ESAstron Dental Corporation · 2011
  2. This deviceK251252 NOBILCAM IMPAK DiscShandong Huge Dental Material Corporation · 2025
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K111828Clearsplint ESAstron Dental Corporation2011—
0 (this device)K251252NOBILCAM IMPAK DiscShandong Huge Dental Material Corporation2025—
FIG. 1 — Lineage of K251252, 2011–2025Source: 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 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 MQC? 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 MQC device

  1. #1 K203000 KeyPrint KeySplint Hardscore 15.3 · 5 generations · 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? (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
*K111828Clearsplint ES
Summary page 5
…Name Reference ASTRON DENTAL Mouthguard, Predicate Clearsplint Disc K111828 MQC CORPORATION Prescription (Primary)…
Astron Dental Corporation2011—
†K003817Pattern ResinGC America, Inc.2001—

Also cleared against K111828: 1 other device →

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.
  • 1 other device also cites its predicate K111828.

How does its category compare?

All MQC devices

MQC Mouthguard, Prescription: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, this device’s year, is highlighted.

FDA decisions per year · MQC

4in 2025

2007: 42009: 22010: 12011: 42012: 22013: 12014: 12015: 32017: 22019: 52020: 42021: 72022: 52023: 62024: 82025: 42026 (partial year): 2
2007high 8 (2024) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MQC

185in 2025

2007: 79 days median2011: 194 days median2015: 234 days median2019: 286 days median2020: 204 days median2021: 158 days median2022: 120 days median2023: 230 days median2024: 249 days median2025: 185 days median
2007high 286 (2019) · low 79 (2007)2026

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

Recalls per year · MQC

1in 2023

2023: 1
2007high 1 (2023) · low 0 (2007)2026

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

Adverse event reports per year · MQC

7in 2025

2007: 92008: 62009: 32010: 52011: 22013: 62014: 22015: 52016: 92017: 72018: 712019: 622020: 462021: 1112022: 1372023: 622024: 82025: 7
2007high 137 (2022) · low 0 (2012)2025

MAUDE reports naming product code MQC, 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
200747909
20080—06
20092—03
20101—05
2011419402
20122—00
20131—06
20141—02
2015323405
20160—09
20172—07
20180—071
20195286062
20204204046
202171580111
202251200137
20236230162
2024824908
2025418507
20262—0—

What is it indicated for?

The NOBILCAM IMPAK Disc is a heat cured, moldable, acrylic compound for use in the fabrication of dental appliances and dental prostheses devices including TMJ splint appliances, nightguards, bruxism appliances and other devices as prescribed.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K251252: NOBILCAM IMPAK Disc.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K251252

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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