Exos, Inc.
Exos, Inc. appears in FDA public data with 0 recalls, 1 510(k) clearance, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 5, 1992.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 1
- Inspections
- 0
- Compliance Actions
- 0
Known Names
exos, exo-s
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K922940 | CLINCAL HAND MASTER SYSTEM MODEL # EXH9000-002 | October 5, 1992 |