Skycade Med Corporation FDA Record
Skycade Med Corporation has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Skycade Med Corporation" is on file.
- Latest 510(k)
- Oct 16, 2026
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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 |
|---|---|---|
| K260168 | Small Diameter Core Wire (CMAN-000-00); Small Diameter Core Wire (CMAN-000-14) | Oct 16, 2026 |
Skycade Med Corporation and the FDA: common questions
Has Skycade Med Corporation received an FDA warning letter?
No FDA warning letter addressed to the name "Skycade Med Corporation" 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 Skycade Med Corporation received an FDA Form 483?
FDA has not published a Form 483 for "Skycade Med Corporation" in its reading room. FDA publishes some Form 483s, not all of them.
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