510(k) · Cleared
ClearedStarband, Starlight
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Orthomerica Products, Inc. · OAN Orthosis, Cranial, Laser Scan
Cleared on Apr 23, 2015 as substantially equivalent to K140353 (Orthomerica Products, Inc., 2014) after a 261-day review. Its family tree reaches back 8 generations to 2000. 1 later device descends from it.
- Decided
- Apr 23, 2015
- Review
- 261 days
- Class
- Class II
- Product code
- OAN
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 8 generations to K001167 (2000). 16 ancestors in all, the oldest DEN980001 (1998). 1 later device descends from it, 1 citing it directly.
- Root · 8 generations backK001167 Opi BandOrthomerica Products, Inc. · 2000
- 7 generations backK021207 StarlightOrthomerica Products, Inc. · 2002
- 6 generations backK081994 StarlightOrthomerica Products, Inc. · 2008
- 5 generations backK082950 StarbandOrthomerica Products, Inc. · 2008
- 4 generations backK111609 Boston BandBoston Brace Intl., Inc. · 2011
- 3 generations backK124023 StarbandOrthomerica Products, Inc. · 2013
- 2 generations backK133250 StarlightOrthomerica Products, Inc. · 2014
- 1 generation backK140353 Starband and StarlightOrthomerica Products, Inc. · 2014
- This deviceK142141 Starband, StarlightOrthomerica Products, Inc. · 2015
- Descendant · cites it directly · 0 of its ownK203098 STARband, STARlight, St. Louis BandOrthomerica Products, Inc. · 2021
Most influential descendants
Showing 1 of 1 · See all- K203098STARband, STARlight, St. Louis BandOrthomerica Products, Inc. · 2021 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −8 | K001167 | Opi Band | Orthomerica Products, Inc. | 2000 | — |
| −7 | K021207 | Starlight | Orthomerica Products, Inc. | 2002 | — |
| −6 | K081994 | Starlight | Orthomerica Products, Inc. | 2008 | — |
| −5 | K082950 | Starband | Orthomerica Products, Inc. | 2008 | — |
| −4 | K111609 | Boston Band | Boston Brace Intl., Inc. | 2011 | — |
| −3 | K124023 | Starband | Orthomerica Products, Inc. | 2013 | — |
| −2 | K133250 | Starlight | Orthomerica Products, Inc. | 2014 | — |
| −1 | K140353 | Starband and Starlight | Orthomerica Products, Inc. | 2014 | — |
| 0 (this device) | K142141 | Starband, Starlight | Orthomerica Products, Inc. | 2015 | — |
| +1 | K203098 | STARband, STARlight, St. Louis Band | Orthomerica Products, Inc. | 2021 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1998 | 1 | 0 |
| 2001 | 1 | 0 |
| 2002 | 1 | 0 |
| 2008 | 3 | 0 |
| 2009 | 2 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2021 | 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 OAN? 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 OAN device
- #1 K244056 DOC Band 3Dscore 9.3 · 2 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 |
|---|---|---|---|
| * | K140353 | Starband and StarlightSummary page 5…ast resistance and creates a precise pathway for the head shape to improve in symmetry and proportion. The STARband and STARlight product families as it was released in K140353 are essentially still the same devices. The STARband Side Opening design and STARband Bi-Valve design is made with an outer shell… | 2014 |
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 |
|---|---|---|---|
| K203098 | STARband, STARlight, St. Louis Band | 2021 | 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 15 years and passes through 2 companies; a new generation was cleared every 1.8 years on median.
- None of the 16 ancestors has a recall.
- Of its descendants, K203098 (Orthomerica Products, Inc., 2021) has gone furthest, with 0 descendants of its own.
- 1 other device also cites its predicate K140353.
How does its category compare?
All OAN devicesOAN Orthosis, Cranial, Laser Scan: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.
FDA decisions per year · OAN
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · OAN
63in 2015
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · OAN
No recall names OAN since 2007.
Adverse event reports per year · OAN
1in 2020
MAUDE reports naming product code OAN, 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 | 1 | — | 0 | 0 |
| 2008 | 5 | 63 | 0 | 0 |
| 2009 | 2 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 1 | — | 0 | 0 |
| 2014 | 1 | — | 0 | 0 |
| 2015 | 3 | 63 | 0 | 0 |
| 2016 | 1 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 1 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 1 |
| 2021 | 2 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 1 | — | 0 | 0 |
| 2025 | 1 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The STARband and STARlight are intended for medical purposes for use on infants from 3 to 18 months of age, with moderate-to-severe non-synostotic positional plagiocephaly, including infants with plagiocephalic-, brachycephalic-, and scaphocephalic-shaped heads by applying mild pressure to prominent regions of the infant's cranium in order to improve cranial symmetry and/or shape. These devices are also indicated for adjunctive use for infants from 3 to 18 months of age whose synostosis has been surgically corrected, but who still have moderate-to-severe cranial deformities including plagiocephalic-, brachycephalic-, and scaphocephalic-shaped heads.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K142141 · printed Nov 6, 2026
Cite this page
510(k) Report. “K142141: Starband, Starlight.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K142141
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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