American Hair Removal System Co. FDA Record
American Hair Removal System Co. has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "American Hair Removal System Co." is on file.
- Latest 510(k)
- Aug 14, 1990
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 |
|---|---|---|
| K892514 | AHRS EPILATOR 629 | Aug 14, 1990 |
American Hair Removal System Co. and the FDA: common questions
Has American Hair Removal System Co. received an FDA warning letter?
No FDA warning letter addressed to the name "American Hair Removal System Co." 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 American Hair Removal System Co. received an FDA Form 483?
FDA has not published a Form 483 for "American Hair Removal System Co." in its reading room. FDA publishes some Form 483s, not all of them.
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