510(k) · Cleared
ClearedIMICRYL Impression Materials
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Imicryl Dis Malzemeleri San. VE Tic. A.S. · ELW Material, Impression
Cleared on Feb 11, 2022 as substantially equivalent to K170736 (Osstem Implant Co., Ltd., 2017) after a 60-day review. Its family tree reaches back 7 generations to 1994.
- Decided
- Feb 11, 2022
- Review
- 60 days
- Class
- Class II
- Product code
- ELW
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 7 generations to K943574 (1994). 14 ancestors in all. No later device cites it as a predicate yet.
- Root · 7 generations backK943574 Capture Impression MaterialDentsply Intl. · 1994
- 6 generations backK973782 Aquasil XLV Smart Wetting Impression MaterialDentsply Intl. · 1997
- 5 generations backK021410 Aquasil Ultra XLV Smart Wetting Impression MaterialDentsply Intl. · 2002
- 4 generations backK082560 Panasil Impression Materials, Including Putty, Binetics, Tray…Kettenbach GmbH & Co. KG · 2008
- 3 generations backK133527 Suflex Putty, Suflex Heavy, Suflex Mono, Suflex LightOsstem Germany GmbH · 2014
- 2 generations backK151262 Hyflex Heavy, Hyflex Mono, Hyflex LightOsstem Implant Co., Ltd. · 2015
- 1 generation backK170736 HySil Impression MaterialsOsstem Implant Co., Ltd. · 2017
- This deviceK213890 IMICRYL Impression MaterialsImicryl Dis Malzemeleri San. VE Tic. A.S. · 2022
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −7 | K943574 | Capture Impression Material | Dentsply Intl. | 1994 | — |
| −6 | K973782 | Aquasil XLV Smart Wetting Impression Material | Dentsply Intl. | 1997 | — |
| −5 | K021410 | Aquasil Ultra XLV Smart Wetting Impression Material | Dentsply Intl. | 2002 | — |
| −4 | K082560 | Panasil Impression Materials, Including Putty, Binetics, Tray, Monophase and… | Kettenbach GmbH & Co. KG | 2008 | — |
| −3 | K133527 | Suflex Putty, Suflex Heavy, Suflex Mono, Suflex Light | Osstem Germany GmbH | 2014 | — |
| −2 | K151262 | Hyflex Heavy, Hyflex Mono, Hyflex Light | Osstem Implant Co., Ltd. | 2015 | — |
| −1 | K170736 | HySil Impression Materials | Osstem Implant Co., Ltd. | 2017 | — |
| 0 (this device) | K213890 | IMICRYL Impression Materials | Imicryl Dis Malzemeleri San. VE Tic. A.S. | 2022 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1996 | 1 | 0 |
| 1997 | 1 | 0 |
| 2002 | 2 | 0 |
| 2005 | 1 | 0 |
| 2010 | 1 | 0 |
| 2016 | 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? (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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K170736 | HySil Impression MaterialsSummary page 6…marketed product: COMPANY DEVICE 510(k) NUMBER PRODUCT CODE Osstem Implant Co., HySil Impression Materials K170736 ELW Ltd. INDICATION FOR USE: SPIRIAS, NICETY, REFLECT and PE Sil Putty Soft is to be used as preliminary mat… | 2017 |
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?
- The line of descent spans 28 years and passes through 5 companies; a new generation was cleared every 4.4 years on median.
- 1 of the 14 ancestors has a recall of any class.
- 5 other devices also cite its predicate K170736.
How does its category compare?
All ELW devicesELW Material, Impression: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, 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?
PUTTY SOFT is to be used as preliminary materials for: -Two-step Putty-wash impression technique -One-step Putty-wash impression technique HEAVY BODY materials for: -One-step impression technique (simultaneous technique) using single or dual viscosities -Two-step impression technique using dual viscosities -Functional impression MEDIUM/MONOPHASE/REGULAR BODY tray or syringeable impression material for: -Taking impressions over fixed/removable…
Read the full statement (185 words)
PUTTY SOFT is to be used as preliminary materials for:
-Two-step Putty-wash impression technique
-One-step Putty-wash impression technique
HEAVY BODY materials for:
-One-step impression technique (simultaneous technique) using single or dual viscosities
-Two-step impression technique using dual viscosities
-Functional impression
MEDIUM/MONOPHASE/REGULAR BODY tray or syringeable impression material for:
-Taking impressions over fixed/removable restorations and implants (i.e., transferring impression posts and bridge components)
-Functional impressions
-Fabricating crown and bridgework or inlays
-Fabricating full or partial dentures
-Reline impressions
-Use in the simultaneous mixing technique as well as the putty-wash and triple tray techniques
-Transferring root posts when fabricating posts and cores indirectly
LIGHT BODY is to be used as syringeable impression materials for:
-Two-step putty-wash impression technique
-One-step putty-wash impression technique
-Two-step impression technique using dual viscosities
-Reline impressions
-Fabricating full or partial dentures
EXTRA LIGHT BODY is to be used as syringeable impression materials for:
-Two-step putty-wash impression technique
-One-step putty-wash impression technique
-Two-step impression technique using dual viscosities
-Reline impressions
-Fabricating full or partial dentures
BITE REGISTRATION is used for impression as below.
-Taking occlusal surfaces
-Confirming occlusal surfaces
-Recording after putting the articulator
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K213890 · printed Nov 6, 2026
Cite this page
510(k) Report. “K213890: IMICRYL Impression Materials.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K213890
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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