Pioneer Surgical Technology, Inc. Dba EXALTA Group FDA Record
- No warning letters matched by name
Pioneer Surgical Technology, Inc. Dba EXALTA Group has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Pioneer Surgical Technology, Inc. Dba EXALTA Group" is on file.
- Latest 510(k)
- Oct 29, 2026
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 11, 2026 (checked Nov 15, 2026, unchanged) | File dated Nov 10, 2026 | Current |
| 510(k) clearances | 1 | Nov 15, 2026 | File dated Nov 9, 2026 | Current |
| Inspections | 0 | Nov 15, 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 |
|---|---|---|
| K262960 | Cerclage Cabling System | Oct 29, 2026 |
Pioneer Surgical Technology, Inc. Dba EXALTA Group and the FDA: common questions
Has Pioneer Surgical Technology, Inc. Dba EXALTA Group received an FDA warning letter?
No FDA warning letter addressed to the name "Pioneer Surgical Technology, Inc. Dba EXALTA Group" 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 Pioneer Surgical Technology, Inc. Dba EXALTA Group received an FDA Form 483?
FDA has not published a Form 483 for "Pioneer Surgical Technology, Inc. Dba EXALTA Group" in its reading room. FDA publishes some Form 483s, not all of them.
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