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Tissue Specialists Resorbable Collagen Membrane
COLLAGEN MATRIX, INC. · Model T5098000 · UDI-DI 00813954028477
NPL
Prescription
10
510(k) clearances
191
Adverse events
11
Recalls
55
Facilities
Description
Resorbable Collagen Membrane For Dental Surgery
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2019-11-05 | Collagen Matrix Inc | The products may have been packaged with an incorrect Instructions for Use. |
| 2019-11-05 | Collagen Matrix Inc | The products may have been packaged with an incorrect Instructions for Use. |
| 2019-11-05 | Collagen Matrix Inc | The products may have been packaged with an incorrect Instructions for Use. |
| 2019-11-05 | Collagen Matrix Inc | The products may have been packaged with an incorrect Instructions for Use. |
| 2019-11-05 | Collagen Matrix Inc | The products may have been packaged with an incorrect Instructions for Use. |
| 2019-11-05 | Collagen Matrix Inc | The products may have been packaged with an incorrect Instructions for Use. |
| 2019-03-19 | Collagen Matrix, Inc. | Product was packaged in the wrong box; may have been placed inside a Neomem FLEXPLUS box instead of a Neomem box |
| 2016-12-02 | Biom'up | Lack of sterility assurance |
| 2012-02-28 | Kensey Nash Corp | Recall has been initiated due to concerns regarding the sterility of the product. The firm initiated the recall because of use of inadequately sterilized product might result in pa |
| 2012-02-28 | Kensey Nash Corp | Recall has been initiated due to concerns regarding the sterility of the product. The firm initiated the recall because of use of inadequately sterilized product might result in pa |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.