Anjon Holdings
Anjon Holdings 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-2778-2020, Class II) was initiated on June 18, 2020. Its most recent 510(k) clearance was granted on March 2, 2020.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-2778-2020 | Class II | Anjon Bremer Molded Crown. bone fixation fastener for spinal use. REF number 100048 - Product Usage | June 18, 2020 |