510(k) · Cleared
ClearedBone and Marrow Collection System Kit
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Biomedical Ent., Inc. · GEY Motor, Surgical Instrument, Ac-Powered
Cleared on Jul 29, 1997 after a 76-day review. FDA’s file for it is a 510(k) statement, which names no predicate.
- Decided
- Jul 29, 1997
- Review
- 76 days
- Class
- Class I
- Product code
- GEY
- Recalls
- None
- Predicates
- 0
FDA’s file for it is a 510(k) statement, which names no predicate.
Sources: FDA 510(k) database (decision fields), the FDA 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in GEY? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
What was it cleared against?
FDA’s file for it is a 510(k) statement, which names no predicate.
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.
How does its category compare?
All GEY devicesGEY Motor, Surgical Instrument, Ac-Powered: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · GEY
FDA has decided no GEY device since 2007.
Median 510(k) review, days · GEY
Too few GEY 510(k)s in any year since 2007 to give a median.
Recalls per year · GEY
2in 2013
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · GEY
965in 2025
MAUDE reports naming product code GEY, 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 | — | 0 | 19 |
| 2008 | 0 | — | 1 | 9 |
| 2009 | 0 | — | 1 | 4 |
| 2010 | 0 | — | 0 | 4 |
| 2011 | 0 | — | 0 | 11 |
| 2012 | 0 | — | 1 | 14 |
| 2013 | 0 | — | 2 | 901 |
| 2014 | 0 | — | 0 | 738 |
| 2015 | 0 | — | 0 | 2,013 |
| 2016 | 0 | — | 0 | 1,943 |
| 2017 | 0 | — | 0 | 2,119 |
| 2018 | 0 | — | 0 | 1,288 |
| 2019 | 0 | — | 0 | 1,131 |
| 2020 | 0 | — | 0 | 952 |
| 2021 | 0 | — | 0 | 1,145 |
| 2022 | 0 | — | 0 | 1,360 |
| 2023 | 0 | — | 0 | 1,444 |
| 2024 | 0 | — | 0 | 1,447 |
| 2025 | 0 | — | 0 | 965 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
To be used with the Bone and Marrow Collection System™ (BMCS). The trocar is used to cut and reflect soft-tissue allowing the BMCS to be placed on bone, the suction connector for converting the BMCS into an aspiration handle and the plunger for extruding tissue from the BMCS.
Indications for use read by OCR from a scanned FDA 510(k) statement, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K971782 · printed Nov 6, 2026
Cite this page
510(k) Report. “K971782: Bone and Marrow Collection System Kit.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K971782
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Page last updated Nov 3, 2026