510(k) · Cleared
ClearedBiomet Microfixation OmniMax MMF System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Biomet Microfixation · JEY Plate, Bone
Cleared on Aug 5, 2021 as substantially equivalent to K152326 (Biomet Microfixation, 2015) after a 309-day review. Its family tree reaches back 7 generations to 1982.
- Decided
- Aug 5, 2021
- Review
- 309 days
- Class
- Class II
- Product code
- JEY
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 7 generations to K820944 (1982). 15 ancestors in all. No later device cites it as a predicate yet.
- Root · 7 generations backK820944 Dental Arch BarUnisplint Corp. · 1982
- 6 generations backK991004 Synthes Quick Lock Imf SystemSynthes (Usa) · 1999
- 5 generations backK031207 Safety Release Arch Bar KitCasey Surgical, LLC · 2003
- 4 generations backK061271 Erch Arch Bar, Model 38-690-00KLS-Martin L.P. · 2006
- 3 generations backK122313 Stryker Universal Smartlock Hybrid MMF SystemStryker · 2012
- 2 generations backK143336 Biomet Microfixation OmniMax MMF SystemBiomet Microfixation · 2015
- 1 generation backK152326 Biomet Microfixation OmniMax MMF SystemBiomet Microfixation · 2015
- This deviceK202969 Biomet Microfixation OmniMax MMF SystemBiomet Microfixation · 2021
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −7 | K820944 | Dental Arch Bar | Unisplint Corp. | 1982 | — |
| −6 | K991004 | Synthes Quick Lock Imf System | Synthes (Usa) | 1999 | — |
| −5 | K031207 | Safety Release Arch Bar Kit | Casey Surgical, LLC | 2003 | — |
| −4 | K061271 | Erch Arch Bar, Model 38-690-00 | KLS-Martin L.P. | 2006 | — |
| −3 | K122313 | Stryker Universal Smartlock Hybrid MMF System | Stryker | 2012 | — |
| −2 | K143336 | Biomet Microfixation OmniMax MMF System | Biomet Microfixation | 2015 | — |
| −1 | K152326 | Biomet Microfixation OmniMax MMF System | Biomet Microfixation | 2015 | — |
| 0 (this device) | K202969 | Biomet Microfixation OmniMax MMF System | Biomet Microfixation | 2021 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1991 | 2 | 0 |
| 1996 | 1 | 0 |
| 1997 | 1 | 0 |
| 1999 | 1 | 0 |
| 2002 | 1 | 0 |
| 2004 | 1 | 0 |
| 2005 | 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 JEY? 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 JEY device
- #1 K252246 Leforte MMF Systemscore 15.6 · 16 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 |
|---|---|---|---|
| * | K152326 | Biomet Microfixation OmniMax MMF SystemSummary page 5…te: Biomet Microfixation Biomet Microfixation OmniMax MMF System OmniMax MMF System (K152326) (K202969) Principle of No change from predicate Metallic implants for the temporar… | 2015 |
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?
- The line of descent spans 39 years and passes through 6 companies; a new generation was cleared every 4.1 years on median.
- None of the 15 ancestors has a recall.
How does its category compare?
All JEY devicesJEY Plate, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.
FDA decisions per year · JEY
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · JEY
159in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · JEY
1in 2020
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · JEY
1,003in 2025
MAUDE reports naming product code JEY, 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 | 9 | 115 | 0 | 29 |
| 2008 | 7 | 84 | 3 | 24 |
| 2009 | 4 | 121 | 6 | 93 |
| 2010 | 6 | 199 | 85 | 215 |
| 2011 | 5 | 75 | 0 | 241 |
| 2012 | 10 | 194 | 0 | 428 |
| 2013 | 8 | 126 | 1 | 766 |
| 2014 | 6 | 223 | 0 | 616 |
| 2015 | 7 | 160 | 0 | 767 |
| 2016 | 1 | — | 0 | 558 |
| 2017 | 5 | 190 | 0 | 568 |
| 2018 | 7 | 255 | 0 | 608 |
| 2019 | 6 | 163 | 0 | 595 |
| 2020 | 6 | 198 | 1 | 680 |
| 2021 | 4 | 299 | 0 | 451 |
| 2022 | 5 | 135 | 0 | 344 |
| 2023 | 2 | — | 0 | 495 |
| 2024 | 5 | 159 | 0 | 696 |
| 2025 | 2 | — | 0 | 1,003 |
| 2026 | 3 | 258 | 0 | — |
What is it indicated for?
The Biomet Microfixation OmniMax MMF System is indicated for temporary stabilization of mandibular and maxillary fractures to maintain proper occlusion during surgery and for post-operative fracture healing in adults and adolescents (age 12 and older) in whom permanent teeth have erupted.
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/K202969 · printed Nov 5, 2026
Cite this page
510(k) Report. “K202969: Biomet Microfixation OmniMax MMF System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K202969
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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