Suite 201, National Innovation Centre FDA Record
- No warning letters matched by name
Suite 201, National Innovation Centre has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Suite 201, National Innovation Centre" is on file.
- Latest 510(k)
- Jul 30, 2026
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 |
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Recent 510(k) clearances
| K-Number | Device | Date |
|---|---|---|
| K261410 | Navbit MARQ (PRD-001-SUP (Supine Registration Kit), PRD-001-LAT (Lateral Registration Kit)) | Jul 30, 2026 |
Suite 201, National Innovation Centre and the FDA: common questions
Has Suite 201, National Innovation Centre received an FDA warning letter?
No FDA warning letter addressed to the name "Suite 201, National Innovation Centre" 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 Suite 201, National Innovation Centre received an FDA Form 483?
FDA has not published a Form 483 for "Suite 201, National Innovation Centre" in its reading room. FDA publishes some Form 483s, not all of them.
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