510(k) · Cleared
ClearedAlginor Alginelle Type 1 and 2 Millenium Kromopan 1 and 2
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Lascod Spa · ELW Material, Impression
Cleared on Aug 23, 2012 after a 63-day review. The FDA summary names its predicate without a number. 3 later devices descend from it.
- Decided
- Aug 23, 2012
- Review
- 63 days
- Class
- Class II
- Product code
- ELW
- Recalls
- None
- Predicates
- 0
3 later devices descend from it, 1 citing it directly.
- This deviceK121824 Alginor Alginelle Type 1 and 2 Millenium Kromopan 1 and 2Lascod Spa · 2012
- Descendant · cites it directly · 2 of its ownK160441 Identic and KromaFaze Alginate Dental Impression MaterialsKerr Corporation · 2016
- Descendant · 2 generations on · 1 of its ownK160097 Image Fast Set, Image Regular SetSybron Dental Specialties · 2016
- Descendant · 2 generations on · 0 of its ownK253501 Hydro Print Premium Fast Set - 454g (1lb) (052037); Hydro Print…Vigodent Indústria E Comercio Ltda · 2025
Most influential descendants
Showing 3 of 3 · See all- K160441Identic and KromaFaze Alginate Dental Impression MaterialsKerr Corporation · 2016 · cites it directly2descendants
- K160097Image Fast Set, Image Regular SetSybron Dental Specialties · 2016 · 2 generations on1descendant
- K253501Hydro Print Premium Fast Set - 454g (1lb) (052037); Hydro Print Premium Regular Set -…Vigodent Indústria E Comercio Ltda · 2025 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K121824 | Alginor Alginelle Type 1 and 2 Millenium Kromopan 1 and 2 | Lascod Spa | 2012 | — |
| +1 | K160441 | Identic and KromaFaze Alginate Dental Impression Materials | Kerr Corporation | 2016 | — |
| +2 | K160097 | Image Fast Set, Image Regular Set | Sybron Dental Specialties | 2016 | — |
| +2 | K253501 | Hydro Print Premium Fast Set - 454g (1lb) (052037); Hydro Print Premium… | Vigodent Indústria E Comercio Ltda | 2025 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2016 | 2 | 0 |
| 2025 | 1 | 0 |
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 ELW? 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 ELW device
- #1 K254152 Dia-X Sil Light Bodyscore 14.1 · 8 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | — | Kromopan 1 Named without a submission number | |
| * | — | Kromopan 2 Named without a submission number |
What descends from it? (3)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K160441 | Identic and KromaFaze Alginate Dental Impression Materials | 2016 | 2 |
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?
- Of its descendants, K160441 (Kerr Corporation, 2016) has gone furthest, with 2 descendants of its own.
How does its category compare?
All ELW devicesELW Material, Impression: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.
FDA decisions per year · ELW
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · ELW
98in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · ELW
3in 2016
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · ELW
22in 2025
MAUDE reports naming product code ELW, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 7 | 60 | 0 | 9 |
| 2008 | 11 | 30 | 0 | 17 |
| 2009 | 7 | 43 | 0 | 7 |
| 2010 | 5 | 88 | 1 | 16 |
| 2011 | 9 | 83 | 0 | 15 |
| 2012 | 7 | 87 | 1 | 14 |
| 2013 | 5 | 67 | 3 | 32 |
| 2014 | 11 | 122 | 0 | 35 |
| 2015 | 8 | 93 | 0 | 18 |
| 2016 | 7 | 166 | 3 | 15 |
| 2017 | 3 | 89 | 0 | 17 |
| 2018 | 5 | 126 | 0 | 14 |
| 2019 | 2 | — | 0 | 24 |
| 2020 | 4 | 99 | 0 | 8 |
| 2021 | 3 | 76 | 0 | 6 |
| 2022 | 7 | 60 | 0 | 9 |
| 2023 | 2 | — | 0 | 13 |
| 2024 | 3 | 98 | 0 | 3 |
| 2025 | 2 | — | 0 | 22 |
| 2026 | 3 | 268 | 0 | — |
What is it indicated for?
Kromopan type 1 and 2, Alginor type 1, Alginelle type 1, Alginelle type 2 and Millenium alginates are irreversible hydrocolloids for dental impressions used by the dentist to take the anatomical data of the patient's mouth and subsequently realize a plaster mold useful to diagnose problems, define the required interventions and/or check their effectiveness. The device is intended to provide models for study and for production of restorative prosthetic devices, such as gold inlays and dentures.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K121824 · printed Nov 6, 2026
Cite this page
510(k) Report. “K121824: Alginor Alginelle Type 1 and 2 Millenium Kromopan 1 and 2.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K121824
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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