Progentix Orthobiology BV FDA Record
Progentix Orthobiology BV has 0 FDA recalls, 0 inspections, 2 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Progentix Orthobiology BV" is on file.
- Latest 510(k)
- Oct 8, 2015
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 2 | 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 |
Recent 510(k) clearances
| K-Number | Device | Date |
|---|---|---|
| K151584 | AttraX Putty | Oct 8, 2015 |
| K090641 | CURIOS | Oct 23, 2009 |
Progentix Orthobiology BV and the FDA: common questions
Has Progentix Orthobiology BV received an FDA warning letter?
No FDA warning letter addressed to the name "Progentix Orthobiology BV" 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 Progentix Orthobiology BV received an FDA Form 483?
FDA has not published a Form 483 for "Progentix Orthobiology BV" in its reading room. FDA publishes some Form 483s, not all of them.
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