510(k) · Cleared
ClearedPEAK
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Neosil Co., Ltd. · ELW Material, Impression
Cleared on Oct 22, 2015 as substantially equivalent to K102836 (Dmp, Ltd., 2011) after a 79-day review. Its family tree reaches back 1 generation to 2011. 1 later device descends from it.
- Decided
- Oct 22, 2015
- Review
- 79 days
- Class
- Class II
- Product code
- ELW
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K102836 (2011). 1 later device descends from it, 1 citing it directly.
Most influential descendants
Showing 1 of 1 · See all- K180565Peak NS033CF, Peak NS017CFNeosil Co., Ltd. · 2018 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K102836 | Bonasil a+ Impression Materials | Dmp, Ltd. | 2011 | — |
| 0 (this device) | K152180 | PEAK | Neosil Co., Ltd. | 2015 | — |
| +1 | K180565 | Peak NS033CF, Peak NS017CF | Neosil Co., Ltd. | 2018 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2018 | 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 |
|---|---|---|---|
| * | K102836 | Bonasil a+ Impression MaterialsSummary page 5…Classification: Class II, 21 CFR 872.3660 Classification Product Code: ELW 4. Predicate Device: BONASIL A+ by DMP, Limited (K102836) 1 5. Device Description: PEAK is a two component (… | 2011 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K180565 | Peak NS033CF, Peak NS017CF | 2018 | 0 |
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?
How does its category compare?
All ELW devicesELW Material, Impression: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, 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?
NS033C is to be used as a light body material for: Two step putty/wash technique Single step putty/wash technique Functional peripheries Silicon dental impressions Crown/bridge work Inlays, Onlays NS017C/NS017T is to be used as a heavy body material for: Two step putty/wash technique Single step putty/wash technique Functional peripheries Crown/bridge work Inlays, Onlays MSP is to be used as a putty body material for: Two step putty/wash technique Single…
Read the full statement (165 words)
NS033C is to be used as a light body material for:
Two step putty/wash technique
Single step putty/wash technique
Functional peripheries
Silicon dental impressions
Crown/bridge work
Inlays, Onlays
NS017C/NS017T is to be used as a heavy body material for:
Two step putty/wash technique
Single step putty/wash technique
Functional peripheries
Crown/bridge work
Inlays, Onlays
MSP is to be used as a putty body material for:
Two step putty/wash technique
Single step putty/wash technique
Functional peripheries
Crown/bridge work
Inlays, Onlays
MSBC is to be used as a bite type for:
Making accurate occlusal registrations
Standards bite registrations in the end bite position.
Key material for needle point registration.
Production of small model segments
MSRC is to be used as a regular body material for:
Two step putty/wash technique
Single step putty/wash technique
Functional peripheries
Reline impressions
Crown/bridge work
Inlays, Onlays
MSCC is to be used as a regular body material for:
Two step putty/wash technique
Single step putty/wash technique
Functional peripheries
Reline impressions
Crown/bridge work
Inlays, Onlays
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K152180 · printed Nov 6, 2026
Cite this page
510(k) Report. “K152180: PEAK.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K152180
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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