510(k) Report

510(k) · Cleared

Cleared

Aidite PMMA

K190217510(k) TraditionalCleared Dec 17, 2020682-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

Aidite (Qinhuangdao) Technology Co., Ltd. · EBG Crown And Bridge, Temporary, Resin

Cleared on Dec 17, 2020 as substantially equivalent to K141421 (Rizhao Huge Dental Industry Co., Ltd., 2015) after a 682-day review. Its family tree reaches back 5 generations to 2007. 1 later device descends from it.

Decided
Dec 17, 2020
Review
682 days
Class
Class II
Product code
EBG
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K070991 (2007). 1 later device descends from it, 1 citing it directly.

  1. Root · 5 generations backK070991 Vita Cad-Temp for Inlab, Model, VX59-4002, VX59-4010, VX59-4102…Vita · 2007
  2. 4 generations backK080182 Zeno Pmma DiscWieland Dental + Technik GmbH & Co. KG · 2008
  3. 3 generations backK122025 Brightglass Brightglass MKtk Medical Supplies GmbH · 2012
  4. 2 generations backK131664 Copra Temp Pmma-DiskWhite Peaks Dental Systems GmbH & Co. KG · 2013
  5. 1 generation backK141421 Pmma BlockRizhao Huge Dental Industry Co., Ltd. · 2015
  6. This deviceK190217 Aidite PMMAAidite (Qinhuangdao) Technology Co., Ltd. · 2020
  7. Descendant · cites it directly · 0 of its ownK223477 PMMA Blocks for Dental UseAidite (Qinhuangdao) Technology Co., Ltd. · 2023

Most influential descendants

Showing 1 of 1 · See all
  • K223477PMMA Blocks for Dental UseAidite (Qinhuangdao) Technology Co., Ltd. · 2023 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K070991Vita Cad-Temp for Inlab, Model, VX59-4002, VX59-4010, VX59-4102, VX59-4110…Vita2007—
−4K080182Zeno Pmma DiscWieland Dental + Technik GmbH & Co. KG2008—
−3K122025Brightglass Brightglass MKtk Medical Supplies GmbH2012—
−2K131664Copra Temp Pmma-DiskWhite Peaks Dental Systems GmbH & Co. KG2013—
−1K141421Pmma BlockRizhao Huge Dental Industry Co., Ltd.2015—
0 (this device)K190217Aidite PMMAAidite (Qinhuangdao) Technology Co., Ltd.2020—
+1K223477PMMA Blocks for Dental UseAidite (Qinhuangdao) Technology Co., Ltd.2023—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202310
FIG. 1 — Lineage of K190217, 2007–2023Source: 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
*K141421Pmma Block
Summary page 4
…Regulation medical specialty Dental 4. Legally Marketed Predicate Devices Trade name PMMA Block 510(K) Number K141421 Manufacturer Rizhao Huge Dental Industry Co., Ltd Device class II…
Rizhao Huge Dental Industry Co., Ltd.2015—

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K223477PMMA Blocks for Dental UseAidite (Qinhuangdao) Technology Co., Ltd.20230

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 13 years and passes through 6 companies; a new generation was cleared every 1.2 years on median.
  • None of the 5 ancestors has a recall.
  • Of its descendants, K223477 (Aidite (Qinhuangdao) Technology Co., Ltd., 2023) has gone furthest, with 0 descendants of its own.

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?

The device is made from PMMA (polymethylmethacrylate) for the fabrication of temporary crowns and bridges and is intended for use in the oral cavity for up to six (6) months while awaiting a permanent restoration. Restorations are designed and manufactured by a dental Professional (Technician) using CAD technology.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K190217: Aidite PMMA.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K190217

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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