Collamatrix Co., Inc. FDA Record
Collamatrix Co., Inc. has 0 FDA recalls, 0 inspections, 6 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Collamatrix Co., Inc." is on file.
- Latest 510(k)
- Jan 3, 2013
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 6 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 0 | Nov 14, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
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Recent 510(k) clearances
| K-Number | Device | Date |
|---|---|---|
| K100695 | COLLADENTAL BARRIER | Jan 3, 2013 |
| K093351 | COLLAWOUND ART | Jun 16, 2010 |
| K090894 | COLLAWOUND WOUND DRESSING | Jun 25, 2009 |
| K071557 | COLLAWOUND HYDROGEL | Feb 8, 2008 |
| K070269 | MODIFICATION TO COLLAWOUND DRESSING | Mar 2, 2007 |
| K061474 | COLLAWOUND DRESSING | Jul 5, 2006 |
Collamatrix Co., Inc. and the FDA: common questions
Has Collamatrix Co., Inc. received an FDA warning letter?
No FDA warning letter addressed to the name "Collamatrix Co., Inc." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.
Has Collamatrix Co., Inc. received an FDA Form 483?
FDA has not published a Form 483 for "Collamatrix Co., Inc." in its reading room. FDA publishes some Form 483s, not all of them.
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