Hefei Meyer Optoelectronic Technology, Inc. FDA Record
Hefei Meyer Optoelectronic Technology, Inc. has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Hefei Meyer Optoelectronic Technology, Inc." is on file.
- Latest 510(k)
- Jul 23, 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 |
|---|---|---|
| K261748 | Dental Cone-beam Computed Tomography (mDX-15P Series) | Jul 23, 2026 |
Hefei Meyer Optoelectronic Technology, Inc. and the FDA: common questions
Has Hefei Meyer Optoelectronic Technology, Inc. received an FDA warning letter?
No FDA warning letter addressed to the name "Hefei Meyer Optoelectronic Technology, Inc." 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 Hefei Meyer Optoelectronic Technology, Inc. received an FDA Form 483?
FDA has not published a Form 483 for "Hefei Meyer Optoelectronic Technology, Inc." in its reading room. FDA publishes some Form 483s, not all of them.
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