510(k) · Cleared
Recalled · 2006Active Life
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Convatec, A Division of E.R. Squibb & Sons · EXB Collector, Ostomy
Cleared on Nov 28, 1983 after a 45-day review. FDA has not posted a summary or statement for it, so its predicates are not known. It has been recalled once.
- Decided
- Nov 28, 1983
- Review
- 45 days
- Class
- Class I
- Product code
- EXB
- Recalls
- 1
- Predicates
- 0
FDA has not posted a summary or statement for it, 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 EXB? 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 EXB device
- #1 K252140 Heylo™ Systemscore 10.4 · 2 generations · no Class I recall
What was it cleared against?
FDA has not posted a summary or statement for it, 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 |
|---|---|---|---|---|
| Jul 13, 2006 | Not classified | Z-1432-06 | Other | Cartons labeled 1-1/4 inch size may contain units that are 1-1/2 inch size. |
No ancestor or descendant has a Class I recall.
How does its category compare?
All EXB devicesEXB Collector, Ostomy: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · EXB
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · EXB
Too few EXB 510(k)s in any year since 2007 to give a median.
Recalls per year · EXB
3in 2011
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · EXB
20in 2025
MAUDE reports naming product code EXB, 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 | 0 |
| 2008 | 0 | — | 2 | 1 |
| 2009 | 0 | — | 0 | 1 |
| 2010 | 0 | — | 0 | 5 |
| 2011 | 0 | — | 3 | 4 |
| 2012 | 0 | — | 0 | 7 |
| 2013 | 0 | — | 0 | 187 |
| 2014 | 1 | — | 0 | 55 |
| 2015 | 0 | — | 0 | 6 |
| 2016 | 0 | — | 0 | 20 |
| 2017 | 0 | — | 0 | 20 |
| 2018 | 1 | — | 0 | 36 |
| 2019 | 0 | — | 0 | 34 |
| 2020 | 0 | — | 0 | 22 |
| 2021 | 0 | — | 0 | 42 |
| 2022 | 0 | — | 0 | 36 |
| 2023 | 0 | — | 0 | 11 |
| 2024 | 0 | — | 0 | 13 |
| 2025 | 1 | — | 0 | 20 |
| 2026 | 0 | — | 0 | — |
https://510kreport.com/device/K833625 · printed Nov 4, 2026
Cite this page
510(k) Report. “K833625: Active Life.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K833625
Report an extraction error
Are you the manufacturer?
Record history
- FDA decision record loaded May 2, 2026
- Page last updated Nov 3, 2026