Retrax Safety Systems, Inc. FDA Record
Retrax Safety Systems, Inc. has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Retrax Safety Systems, Inc." is on file.
- Latest 510(k)
- Jun 2, 2000
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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 | 1 | 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 |
|---|---|---|
| K001017 | RETRAX RETRACTING NEEDLE SYRINGE, SIZE 3CC | Jun 2, 2000 |
Retrax Safety Systems, Inc. and the FDA: common questions
Has Retrax Safety Systems, Inc. received an FDA warning letter?
No FDA warning letter addressed to the name "Retrax Safety Systems, 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 Retrax Safety Systems, Inc. received an FDA Form 483?
FDA has not published a Form 483 for "Retrax Safety Systems, Inc." in its reading room. FDA publishes some Form 483s, not all of them.
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