China Daheng Group Inc.
China Daheng Group Inc. appears in FDA public data with 1 recall, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1145-2014, Class II) was initiated on July 15, 2013. Its most recent 510(k) clearance was granted on November 16, 2011.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-1145-2014 | Class II | Denlase: Diode Laser Therapy System and Penlase: Dental Laser Therapy System surgical powered. | July 15, 2013 |