TissueTech, Inc.
TissueTech, Inc. appears in FDA public data with 3 recalls, 0 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0550-2021, Class II) was initiated on November 10, 2020.
Summary
- Total Recalls
- 3
- 510(k) Clearances
- 0
- Inspections
- 3
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-0550-2021 | Class II | PROKERA, non-sterile - Product Usage: Biologic corneal bandage. | November 10, 2020 |
| Z-0552-2021 | Class II | PROKERA Slim, non-sterile - Product Usage: Biologic corneal bandage. | November 10, 2020 |
| Z-0551-2021 | Class II | PROKERA Plus, non-sterile - Product Usage: Biologic corneal bandage. | November 10, 2020 |