Sunetics International Marketing Group, LLC FDA Record
Sunetics International Marketing Group, LLC has 0 FDA recalls, 0 inspections, 2 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Sunetics International Marketing Group, LLC" is on file.
- Latest 510(k)
- Dec 20, 2013
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 2 | 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 |
|---|---|---|
| K132646 | SUNETICS CLINICAL BIO-STIMULATION LASER | Dec 20, 2013 |
| K121920 | LASERBRUSH | Jun 27, 2013 |
Sunetics International Marketing Group, LLC and the FDA: common questions
Has Sunetics International Marketing Group, LLC received an FDA warning letter?
No FDA warning letter addressed to the name "Sunetics International Marketing Group, LLC" 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 Sunetics International Marketing Group, LLC received an FDA Form 483?
FDA has not published a Form 483 for "Sunetics International Marketing Group, LLC" in its reading room. FDA publishes some Form 483s, not all of them.
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