510(k) · Cleared
ClearedModel 672-BD, Home Uvb Light Source (Jordan Light); Model 2400, 4 (6 Foot) HO UV Light Source; Model 2600, 6 (6 Foot) HO
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
The Richmond Light Co. · FTC Light, Ultraviolet, Dermatological
Cleared on Oct 17, 2005 as substantially equivalent to K812446 (The Richmond Light Co., 1981) and 2 other predicates after a 20-day review. Its family tree reaches back 1 generation to 1981.
- Decided
- Oct 17, 2005
- Review
- 20 days
- Class
- Class II
- Product code
- FTC
- Recalls
- None
- Predicates
- 5
Its longest line of descent runs back 1 generation to K812446 (1981). 3 ancestors in all. No later device cites it as a predicate yet.
- Root · 1 generation backK812446 SunlampThe Richmond Light Co. · 1981
- This deviceK052660 Model 672-BD, Home Uvb Light Source (Jordan Light); Model 2400, 4 (6…The Richmond Light Co. · 2005
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K812446 | Sunlamp | The Richmond Light Co. | 1981 | — |
| 0 (this device) | K052660 | Model 672-BD, Home Uvb Light Source (Jordan Light); Model 2400, 4 (6 Foot) HO… | The Richmond Light Co. | 2005 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1985 | 1 | 0 |
| 1990 | 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 FTC? 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 FTC device
- #1 K242977 308nm Excimer Phototherapy Device (CN-308E…score 14.8 · 21 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (5)
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; numbers the summary cites that cannot be its predicate are marked – and kept off the family tree.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K812446 | SunlampSummary page 1…at, to the best of its knowledge, the proposed family has the same use and similar technical characteristics as the predicate devices: The Richmond Light Co., Inc. 648B (K8 12446), the National Biological Panasol 4 and 6 foot units (K904426, -27, -28), and the Daavlin Spectra 724 Series, Ultraviolet Phototh… | 1981 |
| * | K904426 | Panosol II Uva-218Summary page 1…ame use and similar technical characteristics as the predicate devices: The Richmond Light Co., Inc. 648B (K8 12446), the National Biological Panasol 4 and 6 foot units (K904426, -27, -28), and the Daavlin Spectra 724 Series, Ultraviolet Phototherapy Device (K854498) The submitted devices can be demonstra… | 1990 |
| Kept off the family tree | K904427 | FDA’s K904427 is Panosol II Uvb-206 Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree | 1990 |
| Kept off the family tree | K904428 | FDA’s K904428 is Panosol II Uab-228 Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree | 1990 |
| * | K854498 | Spectra 724Summary page 1…t Co., Inc. 648B (K8 12446), the National Biological Panasol 4 and 6 foot units (K904426, -27, -28), and the Daavlin Spectra 724 Series, Ultraviolet Phototherapy Device (K854498) The submitted devices can be demonstrated to be as safe and effective as the legally marketed predicate devices and do not vary… | 1985 |
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?
- None of the 3 ancestors has a recall.
How does its category compare?
All FTC devicesFTC Light, Ultraviolet, Dermatological: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · FTC
3in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · FTC
76in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · FTC
3so far in 2026, the most since 2007
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · FTC
8in 2025
MAUDE reports naming product code FTC, 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 | 4 | 53 | 0 | 0 |
| 2008 | 3 | 41 | 1 | 0 |
| 2009 | 2 | — | 0 | 0 |
| 2010 | 1 | — | 0 | 2 |
| 2011 | 5 | 125 | 0 | 0 |
| 2012 | 1 | — | 0 | 1 |
| 2013 | 1 | — | 0 | 1 |
| 2014 | 2 | — | 0 | 1 |
| 2015 | 3 | 98 | 0 | 8 |
| 2016 | 1 | — | 0 | 2 |
| 2017 | 2 | — | 0 | 2 |
| 2018 | 3 | 88 | 0 | 0 |
| 2019 | 2 | — | 0 | 14 |
| 2020 | 5 | 237 | 0 | 4 |
| 2021 | 3 | 89 | 0 | 48 |
| 2022 | 1 | — | 0 | 4 |
| 2023 | 4 | 48 | 0 | 5 |
| 2024 | 1 | — | 0 | 4 |
| 2025 | 3 | 76 | 1 | 8 |
| 2026 | 4 | 91 | 3 | — |
What is it indicated for?
All Models in this submission are phototherapy products designed for individuals who require specific Ultraviolet radiation therapy for the treatment of psoriasis..
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K052660 · printed Nov 6, 2026
Cite this page
510(k) Report. “K052660: Model 672-BD, Home Uvb Light Source (Jordan Light); Model 2400, 4 (6 Foot) HO UV Light Source; Model 2600, 6 (6 Foot) HO.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K052660
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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