Uscom Limited
FDA Regulatory Profile
Uscom Limited has 0 FDA recalls, 4 inspections, 1 510(k) clearance and 0 compliance actions on record.
- Latest inspection
- May 29, 2025 · VAI
- Latest 510(k)
- Feb 15, 2005
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Summary
Record counts and when each FDA source was last refreshed
| 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 | 4 | Nov 11, 2026 | Newest record Nov 5, 2026 | Current |
|---|
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
|---|
Related names
| Name | Recalls | 510(k) | Inspections | Compliance | Most recent recall |
|---|
Uscom Kft
Same company group | 0 | 0 | 1 | 1 | — |
Recent FDA Inspections
NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|
| FEI 3004987887 | Sydney, Australia | 4 | May 29, 2025 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K043139 | USCOM 1A | Feb 15, 2005 |