510(k) Report

510(k) · Cleared

Cleared

PMMA Block

K201683510(k) TraditionalCleared Nov 3, 2020134-day reviewClass II21 CFR 872.3770

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

Huge Dental Material Co., Ltd. · EBG Crown And Bridge, Temporary, Resin

Cleared on Nov 3, 2020 as substantially equivalent to K150432 (Union Dental S.A., 2015) after a 134-day review. Its family tree reaches back 4 generations to 1994. 2 later devices descend from it.

Decided
Nov 3, 2020
Review
134 days
Class
Class II
Product code
EBG
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K924830 (1994). 5 ancestors in all. 2 later devices descend from it, 1 citing it directly.

  1. Root · 4 generations backK924830 Luxatemp AutomixDmg Chemisch Pharmazeutische Fabrik GmbH · 1994
  2. 3 generations backK060293 Temporary Crown and Bridge MaterialDentsply International, Inc. · 2006
  3. 2 generations backK071548 Wieland Zeno Cao Temporary Pmma Disc, Tooth-ColoredMerz Dental GmbH · 2007
  4. 1 generation backK150432 Idodentine Disc, Idodentine BlockUnion Dental S.A. · 2015
  5. This deviceK201683 PMMA BlockHuge Dental Material Co., Ltd. · 2020
  6. Descendant · cites it directly · 1 of its ownK223706 Pmma BlockHuliang (Shanghai) Bio-Tech Co., Ltd. · 2023
  7. Descendant · 2 generations on · 0 of its ownK253380 “FLNT Base” and “FLNT Temp”Liaoning Upcera Co., Ltd. · 2026

Most influential descendants

Showing 2 of 2 · See all
  • K223706Pmma BlockHuliang (Shanghai) Bio-Tech Co., Ltd. · 2023 · cites it directly1descendant
  • K253380“FLNT Base” and “FLNT Temp”Liaoning Upcera Co., Ltd. · 2026 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K924830Luxatemp AutomixDmg Chemisch Pharmazeutische Fabrik GmbH1994—
−3K060293Temporary Crown and Bridge MaterialDentsply International, Inc.2006—
−2K071548Wieland Zeno Cao Temporary Pmma Disc, Tooth-ColoredMerz Dental GmbH2007—
−1K150432Idodentine Disc, Idodentine BlockUnion Dental S.A.2015—
0 (this device)K201683PMMA BlockHuge Dental Material Co., Ltd.2020—
+1K223706Pmma BlockHuliang (Shanghai) Bio-Tech Co., Ltd.2023—
+2K253380“FLNT Base” and “FLNT Temp”Liaoning Upcera Co., Ltd.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202310
202610
FIG. 1 — Lineage of K201683, 1994–2026Source: 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 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 EBG? 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 EBG device

  1. #1 K253380 “FLNT Base” and “FLNT Temp”score 12.4 · 6 generations · 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
*K150432Idodentine Disc, Idodentine Block
Summary page 4
…Decision Date Primary Union Dental IDODENTINE Dental Predicate K150432 08/14/2015 EBG, EBI, S.A. Polymer Blank…
Union Dental S.A.2015—
†K141421Pmma BlockRizhao Huge Dental Industry Co., Ltd.2015—

Also cleared against K150432: 5 other devices →

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K223706Pmma BlockHuliang (Shanghai) Bio-Tech Co., Ltd.20231

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 26 years and passes through 5 companies; a new generation was cleared every 8.0 years on median.
  • None of the 5 ancestors has a recall.
  • Of its descendants, K223706 (Huliang (Shanghai) Bio-Tech Co., Ltd., 2023) has gone furthest, with 1 descendant of its own.
  • 5 other devices also cite its predicate K150432.

How does its category compare?

All EBG devices

EBG Crown And Bridge, Temporary, Resin: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · EBG

4in 2025

2007: 32008: 92009: 22010: 52011: 102012: 52013: 22014: 32015: 62016: 42017: 22018: 42019: 62020: 142021: 32022: 32023: 22024: 52025: 42026 (partial year): 2
2007high 14 (2020) · low 2 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EBG

106in 2025

2007: 64 days median2008: 83 days median2010: 103 days median2011: 96 days median2012: 90 days median2014: 114 days median2015: 209 days median2016: 163 days median2018: 202 days median2019: 98 days median2020: 194 days median2021: 265 days median2022: 73 days median2024: 144 days median2025: 106 days median
2007high 265 (2021) · low 64 (2007)2026

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

Recalls per year · EBG

1in 2020

2009: 12020: 1
2007high 1 (2009) · low 0 (2007)2026

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

Adverse event reports per year · EBG

1in 2025

2007: 42008: 42009: 12010: 12011: 12012: 52013: 112014: 232015: 262016: 82017: 42019: 62020: 22021: 42022: 22025: 1
2007high 26 (2015) · low 0 (2018)2025

MAUDE reports naming product code EBG, 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
200736404
200898304
20092—11
2010510301
2011109601
201259005
20132—011
20143114023
20156209026
2016416308
20172—04
2018420200
201969806
20201419412
2021326504
202237302
20232—00
2024514400
2025410601
20262—0—

What is it indicated for?

PMMA BLOCK particularly suitable for making removable or temporary dental structures such as crowns and bridges using milling technology using CAD/CAM.

Indications for Use:

- Temporary anterior and posterior crowns;

- Temporary anterior and posterior bridges;

- Implant surgical guide;

- Removable structures for dentures;

- Removable structures for therapeutic restorations (night guards, bite splints or occlusal splints).

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K201683: PMMA Block.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K201683

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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