510(k) · Cleared
ClearedFir Heat Theraphy Sysyems
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Shenzhen Anpan Technology Co., Ltd. · IRT Pad, Heating, Powered
Cleared on Nov 8, 2011 as substantially equivalent to K092589 (Eas Consulting Group, LLC, 2010) after a 188-day review. Its family tree reaches back 2 generations to 2008. 1 later device descends from it.
- Decided
- Nov 8, 2011
- Review
- 188 days
- Class
- Class II
- Product code
- IRT
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 2 generations to K072534 (2008). 1 later device descends from it, 1 citing it directly.
- Root · 2 generations backK072534 Bio-Mat 2000Richway Intl., Inc. · 2008
- 1 generation backK092589 Thermotex Platinum SystemEas Consulting Group, LLC · 2010
- This deviceK111273 Fir Heat Theraphy SysyemsShenzhen Anpan Technology Co., Ltd. · 2011
- Descendant · cites it directly · 0 of its ownK133981 Avacen 100Avacen, Inc. · 2014
Most influential descendants
Showing 1 of 1 · See all- K133981Avacen 100Avacen, Inc. · 2014 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K072534 | Bio-Mat 2000 | Richway Intl., Inc. | 2008 | — |
| −1 | K092589 | Thermotex Platinum System | Eas Consulting Group, LLC | 2010 | — |
| 0 (this device) | K111273 | Fir Heat Theraphy Sysyems | Shenzhen Anpan Technology Co., Ltd. | 2011 | — |
| +1 | K133981 | Avacen 100 | Avacen, Inc. | 2014 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2014 | 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 IRT? 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 IRT device
- #1 K250047 bite away twoscore 10.6 · 3 generations · no Class I recall
- #2 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 |
|---|---|---|---|
| * | K092589 | Thermotex Platinum SystemSummary page 2…n Sponsor: EAS Consulting Group LLC. Device Name: Thermotex Heat Therapy Systems 510(k) Number: K092589 Product Code: IRT, ILY Regulation Number: CFR 890.5740, 890.5500 Regulation Class:… | 2010 |
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 |
|---|---|---|---|
| K133981 | Avacen 100 | 2014 | 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?
- The line of descent spans 3 years and passes through 3 companies; a new generation was cleared every 2.0 years on median.
- None of the 2 ancestors has a recall.
- Of its descendants, K133981 (Avacen, Inc., 2014) has gone furthest, with 0 descendants of its own.
- 2 other devices also cite its predicate K092589.
How does its category compare?
All IRT devicesIRT Pad, Heating, Powered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.
FDA decisions per year · IRT
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · IRT
Too few IRT 510(k)s in any year since 2007 to give a median.
Recalls per year · IRT
3in 2022
Class I (3 since 2007) Class II/III not classified
Adverse event reports per year · IRT
70in 2025
MAUDE reports naming product code IRT, 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 | 0 | — | 5 | 312 |
| 2008 | 1 | — | 0 | 242 |
| 2009 | 0 | — | 0 | 555 |
| 2010 | 0 | — | 0 | 413 |
| 2011 | 1 | — | 0 | 227 |
| 2012 | 0 | — | 0 | 233 |
| 2013 | 0 | — | 0 | 345 |
| 2014 | 1 | — | 0 | 414 |
| 2015 | 1 | — | 0 | 289 |
| 2016 | 1 | — | 1 | 182 |
| 2017 | 0 | — | 0 | 220 |
| 2018 | 0 | — | 0 | 325 |
| 2019 | 0 | — | 0 | 205 |
| 2020 | 0 | — | 0 | 117 |
| 2021 | 0 | — | 0 | 97 |
| 2022 | 1 | — | 3 (3) | 134 |
| 2023 | 0 | — | 0 | 321 |
| 2024 | 0 | — | 0 | 77 |
| 2025 | 1 | — | 0 | 70 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The FIR Heat Therapy Systems are indicated for the temporary relief of minor muscle and joint pain and stiffness; the temporary relief of joint pain associated with arthritis, muscle spasms, minor strains and sprains and minor muscular back pain; muscular relaxation; and the temporary increase of local circulation where applied.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K111273 · printed Nov 6, 2026
Cite this page
510(k) Report. “K111273: Fir Heat Theraphy Sysyems.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K111273
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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