Facility
M-SOLUTIONS INC.
1 recall(s) on record — most severe on record: Class II.
| FDA Establishment Identifier (FEI) | 3013875850 |
|---|---|
| Establishment type | Export Device to the United States But Perform No Other Operation on Device |
| Location | 2-16-2 MinamiShinozakiMachi Tokyo, JP 13300 |
| Registration status | Active · expires 2026 |
| Parent company | M-solutions Inc. (owner-operator 10055621) |
Devices registered here (1)
- Device, Beam Limiting, X-Ray, DiagnosticProduct code KPW · Class II · Radiology · 21 CFR 892.1610
Recalls & enforcement
- Class IITerminated2016-11-22Product malfunction: Needle does not retract.
Related
Source: U.S. FDA via openFDA (device registration & enforcement). Data as of 2026-08-13. Verify this facility record at FDA →
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