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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 1 of 5| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Fixed Case | MRS-104-01 | EUDAMEDFDA UDI | Class I | Active |
| Bradshaw Medical Inc. | CW-0025-ATEC | FDA UDI | Class I | Active |
| Modular Retractor System | MRS-100 | FDA UDI | Class I | Active |
| Mobile Case | MRS-104-02 | EUDAMEDFDA UDI | Class I | Active |
| Rod-Gripper Lumbar Dual Action 5.5mm Silicone Overmold | RGV-01-01-550-00-A | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0215 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0102 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0110 | FDA UDI | Class I | Active |
| Bradshaw Medical, Inc. | 925-0311 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0108 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0205 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | NR-501008DG-ATEC | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0701 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0112 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0110 | FDA UDI | Class I | Active |
| Base 1 | MRS-116-01-02 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0401 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0113 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | IC-000070 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0203 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0801 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-1004 | FDA UDI | Class I | Active |
| Plate blade without teeth - length 90 mm | MRS-110-090 | FDA UDI | Class I | Active |
| Bradshaw Medical, Inc. | 925-0321 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0805 | FDA UDI | Class I | Active |
| 5.5mm LUMBAR ROD GRIPPER | LRG-602-001 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0108 | FDA UDI | Class I | Active |
| TORO, MEDIUM AXIAL, 3.5mm HEX | 804-06-009 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0703 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0101 | FDA UDI | Class I | Active |
| Plate blade without teeth - length 110 mm | MRS-110-110 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-1004 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0408 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0104 | FDA UDI | Class I | Active |
| Concentrical blade - length 50 mm | MRS-108-050 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0502 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0905 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0904 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0206 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | CW-0030-ATEC | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0901 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | RIV-12-18-02DG-ATEC | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0904 | FDA UDI | Class I | Active |
| Bradshaw Medical, Inc. | 925-0314 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0105 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 925-0303 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | 920-0307 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | IC-000071 | FDA UDI | Class I | Active |
| Bradshaw Medical Inc. | WR-000001DG-ATEC | FDA UDI | Class I | Active |
| Bradshaw Medical | HRC212312 | 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. |