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Sign in to claim this brandBradshaw Medical Inc.
United States·US-MF-000003392
Last updated September 17, 2026
Information
- Country
- United States
- Address
- 10325 58th Place, Kenosha, United States
- Website
- www.exalta.com
- —
- —
- [email protected]
- Phone
- —
- PRRC Contact
- Tania Shammo
- EUDAMED SRN
- US-MF-000003392
- FDA FEI Number
- 3006846753
- DUNS Number
- —
Catalogue (215)
Page 2 of 5| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bradshaw Medical Inc. | 920-0308 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc | 925-0323 | FDA UDI | Class I | Active |
| Concentrical blade - length 130 mm | MRS-108-130 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | ES-000002DG-ATEC | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | RIV-15-11-01DG-ATEC | FDA UDI | Class I | Active |
| Plate blade with teeth - length 80 mm | MRS-109-080 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0103 | FDA UDI | Class I | Active |
| Dilator 1 | MRS-107-1 | FDA UDI | Class I | Active |
| Rack | MRS-101 | EUDAMEDFDA UDI | Class I | Active |
| Tray 2 | MRS-116-02-02 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0326 | FDA UDI | Class I | Active |
| Bradshaw Medical, Inc. | 925-0315 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0906 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0601 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0404 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 5161-00-5019 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0501 | FDA UDI | Class I | Active |
| Plate blade with teeth - length 90 mm | MRS-109-090 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0115 | FDA UDI | Class I | Active |
| Concentrical blade - length 70 mm | MRS-108-070 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0210 | FDA UDI | Class I | Active |
| Concentrical blade - length 100 mm | MRS-108-100 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0304 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0201 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0601 | FDA UDI | Class I | Active |
| Bradshaw Medical, Inc. | 925-0312 | FDA UDI | Class I | Active |
| Concentrical blade - length 90 mm | MRS-108-090 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0113 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0302 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0802 | FDA UDI | Class I | Active |
| Plate blade with teeth - length 120 mm | MRS-109-120 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | RG-000505DG-ATEC | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-1005 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | IC-000073 | FDA UDI | Class I | Active |
| Plate blade without teeth - length 50 mm | MRS-110-050 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0903 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-1001 | FDA UDI | Class I | Active |
| Concentrical blade - length 60 mm | MRS-108-060 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-1002 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0208 | FDA UDI | Class I | Active |
| Concentrical blade - length 120 mm | MRS-108-120 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | ES-000004DG-ATEC | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0111 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0304 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0209 | FDA UDI | Class I | Active |
| Lid 2 | MRS-116-02-01 | FDA UDI | Class I | Active |
| Bradshaw Medical, Inc. | 925-0325 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0403 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-1102 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0107 | FDA UDI | Class I | Active |
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Feb 2, 2015 | Z-1637-2016 | — | terminated | A component failure could cause a situation where the applied torque was significantly higher than the calibrated torque setting. |