510(k) · Cleared
Recalled · Class II · 2013Fray Bio-Punch
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Fray Products Corp. · MDM Instrument, Manual, Surgical, General Use
Cleared on Oct 28, 1992 after a 195-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. It has been recalled 3 times.
- Decided
- Oct 28, 1992
- Review
- 195 days
- Class
- Class I
- Product code
- MDM
- Recalls
- 3
- Predicates
- 0
FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.
Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in MDM? 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Mar 18, 2013 | Class II | Z-1654-2013 | Packaging change control | Due to lack of sterilization. |
| Mar 18, 2013 | Class II | Z-1655-2013 | Packaging change control | Due to lack of sterilization. |
| Mar 18, 2013 | Class II | Z-1656-2013 | Packaging change control | Due to lack of sterilization. |
No ancestor or descendant has a Class I recall.
How does its category compare?
All MDM devicesMDM Instrument, Manual, Surgical, General Use: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · MDM
1in 2008
2026 to Oct 25, outlined.
Median 510(k) review, days · MDM
Too few MDM 510(k)s in any year since 2007 to give a median.
Recalls per year · MDM
1in 2024
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · MDM
318in 2025
MAUDE reports naming product code MDM, 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 | 25 |
| 2008 | 1 | — | 0 | 50 |
| 2009 | 0 | — | 1 | 131 |
| 2010 | 0 | — | 17 | 49 |
| 2011 | 0 | — | 1 | 52 |
| 2012 | 0 | — | 0 | 53 |
| 2013 | 0 | — | 0 | 74 |
| 2014 | 0 | — | 1 | 66 |
| 2015 | 0 | — | 0 | 161 |
| 2016 | 0 | — | 0 | 317 |
| 2017 | 0 | — | 2 | 187 |
| 2018 | 0 | — | 0 | 400 |
| 2019 | 0 | — | 0 | 281 |
| 2020 | 0 | — | 0 | 245 |
| 2021 | 0 | — | 1 | 227 |
| 2022 | 0 | — | 2 | 182 |
| 2023 | 0 | — | 0 | 209 |
| 2024 | 0 | — | 1 | 507 |
| 2025 | 0 | — | 0 | 318 |
| 2026 | 0 | — | 1 | — |
https://510kreport.com/device/K921822 · printed Nov 5, 2026
Cite this page
510(k) Report. “K921822: Fray Bio-Punch.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K921822
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Record history
- FDA decision record loaded May 2, 2026
- Page last updated Nov 3, 2026