510(k) · Decided
DecidedOrbit Subretinal Delivery System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Orbit Biomedical, Inc. · FMF Syringe, Piston
Cleared on Nov 20, 2018 as substantially equivalent to K023752 (Bd, 2003) after a 90-day review. Its family tree reaches back 2 generations to 1998. 4 later devices descend from it.
- Decided
- Nov 20, 2018
- Review
- 90 days
- Class
- Class II
- Product code
- FMF
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 2 generations to K980069 (1998). 4 ancestors in all. 4 later devices descend from it, 1 citing it directly.
- Root · 2 generations backK980069 Vanishpoint SyringeRetractable Technologies, Inc. · 1998
- 1 generation backK023752 BD Integra SyringeBd · 2003 · Recalled
- This deviceK182274 Orbit Subretinal Delivery SystemOrbit Biomedical, Inc. · 2018
- Descendant · cites it directly · 3 of its ownK200325 Orbit Subretinal Delivery SystemOrbit Biomedical · 2020
- Descendant · 2 generations on · 2 of its ownK203264 MicroDose InjectorMedone Surgical, Inc. · 2021
- Descendant · 2 generations on · 1 of its ownK213467 EVA NEXUS Ophthalmic Surgical SystemD.O.R.C. Dutch Ophthalmic Research Center (International) · 2022 · Recalled
- Descendant · 3 generations on · 0 of its ownK250501 System SophiThis AG · 2025
Most influential descendants
Showing 4 of 4 · See all- K200325Orbit Subretinal Delivery SystemOrbit Biomedical · 2020 · cites it directly3descendants
- K203264MicroDose InjectorMedone Surgical, Inc. · 2021 · 2 generations on2descendants
- K213467EVA NEXUS Ophthalmic Surgical SystemD.O.R.C. Dutch Ophthalmic Research Center (International) · 2022 · 2 generations on1descendant
- K250501System SophiThis AG · 2025 · 3 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K980069 | Vanishpoint Syringe | Retractable Technologies, Inc. | 1998 | — |
| −1 | K023752 | BD Integra Syringe | Bd | 2003 | 2 |
| 0 (this device) | K182274 | Orbit Subretinal Delivery System | Orbit Biomedical, Inc. | 2018 | — |
| +1 | K200325 | Orbit Subretinal Delivery System | Orbit Biomedical | 2020 | — |
| +2 | K203264 | MicroDose Injector | Medone Surgical, Inc. | 2021 | — |
| +2 | K213467 | EVA NEXUS Ophthalmic Surgical System | D.O.R.C. Dutch Ophthalmic Research Center (International) | 2022 | 6 |
| +3 | K250501 | System Sophi | This AG | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1998 | 1 | 0 |
| 2001 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2020 | 1 | 0 |
| 2021 | 1 | 0 |
| 2022 | 1 | 0 |
| 2025 | 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 FMF? 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 FMF device
- #1 K241821 Luer Lock Syringe with Safety Needle; Luer…score 16.2 · 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.
What descends from it? (4)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K200325 | Orbit Subretinal Delivery System | 2020 | 3 |
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 20 years and passes through 3 companies; a new generation was cleared every 15.8 years on median.
- 1 of the 4 ancestors has a recall of any class.
- Of its descendants, K200325 (Orbit Biomedical, 2020) has gone furthest, with 3 descendants of its own.
- 4 other devices also cite its predicate K023752.
How does its category compare?
All FMF devicesFMF Syringe, Piston: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.
FDA decisions per year · FMF
13in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · FMF
114in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · FMF
19in 2023
Class I (19 since 2007) Class II/III not classified
Adverse event reports per year · FMF
4,181in 2025
MAUDE reports naming product code FMF, 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 | 23 | 90 | 6 | 674 |
| 2008 | 9 | 74 | 11 | 691 |
| 2009 | 14 | 94 | 15 | 913 |
| 2010 | 11 | 130 | 12 | 679 |
| 2011 | 16 | 109 | 3 | 186 |
| 2012 | 9 | 86 | 6 | 307 |
| 2013 | 12 | 154 | 1 | 326 |
| 2014 | 13 | 84 | 1 | 244 |
| 2015 | 11 | 87 | 2 | 273 |
| 2016 | 12 | 146 | 0 | 684 |
| 2017 | 13 | 135 | 3 | 1,858 |
| 2018 | 8 | 87 | 2 | 3,952 |
| 2019 | 11 | 146 | 1 | 5,863 |
| 2020 | 15 | 107 | 2 | 5,334 |
| 2021 | 20 | 175 | 1 | 5,874 |
| 2022 | 24 | 211 | 2 | 5,233 |
| 2023 | 22 | 173 | 19 (18) | 5,214 |
| 2024 | 14 | 130 | 0 | 5,122 |
| 2025 | 13 | 114 | 0 | 4,181 |
| 2026 | 9 | 239 | 2 (1) | — |
What is it indicated for?
The Orbit Subretinal Delivery System is indicated for microinjection into the subretinal space.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K182274 · printed Nov 4, 2026
Cite this page
510(k) Report. “K182274: Orbit Subretinal Delivery System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K182274
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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