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Sign in to claim this brandMiami Device Solutions
US
Last updated May 23, 2026
What Miami Device Solutions makes
Miami Device Solutions manufactures orthopaedic fixation devices including non-bioabsorbable plates and bone screws, internal fixation systems combining plates and screws, and reusable surgical instruments such as drill guides, depth gauges, aiming blocks, and implant inserters/extractors. The company also produces instrument transport trolleys and related hardware like plate holders and torque limiter handles.
All devices are classified as Class II and are listed in the FDA's Unique Device Identification (FDA UDI) system. The company is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of devices does Miami Device Solutions manufacture?
Miami Device Solutions manufactures orthopaedic fixation devices such as non-bioabsorbable plates and bone screws, internal fixation systems combining plates and screws, and reusable surgical instruments including drill guides, depth gauges, aiming blocks, and implant inserters/extractors. The company also produces instrument transport trolleys and related hardware like plate holders and torque limiter handles, all based on the provided device data.
Where is Miami Device Solutions based?
Miami Device Solutions is based in the United States, as explicitly stated in the device data under the COUNTRY field, which specifies US as the country of origin for the manufacturer.
Which regulatory registries list the devices made by Miami Device Solutions?
The devices manufactured by Miami Device Solutions are listed in the FDA's Unique Device Identification (FDA UDI) system, as indicated in the LISTED IN field of the device data, which specifies fda_udi as the registry where their devices are registered.
How are the devices made by Miami Device Solutions classified?
All devices produced by Miami Device Solutions are classified as Class II, as stated in the DEVICE CLASSES field of the device data, which uniformly assigns Class II to every device category and example listed.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
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Catalogue (471)
Page 4 of 10| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Distal Humerus Plate, Posterolateral | MDS170103LP | FDA UDI | Class II | Active |
| Olecranon Plate, 2 Hole, Right | MDS160102R | FDA UDI | Class II | Active |
| Peg, 1.8mm | MDS1902P16 | FDA UDI | Class II | Active |
| Narrow Plate, 2.7T | MDS1001N20 | FDA UDI | Class II | Active |
| Distal Humerus Plate, Posterolateral | MDS170103RP | FDA UDI | Class II | Active |
| Cortical Screw, 2.7mm | MDS1002X14 | FDA UDI | Class II | Active |
| Multiuse Screw, 2.7mm | MDS1002M48 | FDA UDI | Class II | Active |
| Cortical Screw, 2.7mm | MDS1002X10 | FDA UDI | Class II | Active |
| Cannulated Screw, 3.5mm | MDS1102MC60 | FDA UDI | Class II | Active |
| Extra Articular Distal Humerus Plate | MDS170110R | FDA UDI | Class II | Active |
| Proximal Humerus Plate | MDS130108R | FDA UDI | Class II | Active |
| Narrow Plate, 3.5T | MDS1101N14 | FDA UDI | Class II | Active |
| Cortical Screw Tap, Ø3.5mm | MDS110825UAO | FDA UDI | Class II | Active |
| Cortical Screw, 2.7mm | MDS1002X42 | FDA UDI | Class II | Active |
| Peg, 1.8mm | MDS1902P08 | FDA UDI | Class II | Active |
| Multiuse Screw, 3.5mm | MDS1102M54 | FDA UDI | Class II | Active |
| Narrow Plate, 2.7T | MDS1001N17 | FDA UDI | Class II | Active |
| Locking Cap Block, Narrow | MDS140903 | FDA UDI | Class II | Active |
| Cortical Screw, 2.7mm | MDS1002X62 | FDA UDI | Class II | Active |
| Peg, 1.8mm | MDS1902P19 | FDA UDI | Class II | Active |
| Peg, 1.8mm | MDS1902P14 | FDA UDI | Class II | Active |
| Narrow Plate, 3.5T | MDS1101N04 | FDA UDI | Class II | Active |
| 2.5mm Drill | MDS111125150 | FDA UDI | Class II | Active |
| MDS Plating System Instrument Tray Bottom | MDS11120402 | FDA UDI | Class II | Active |
| Broad Plate, 3.5T | MDS1101B18 | FDA UDI | Class II | Active |
| Multiuse Screw, 3.5mm | MDS1102M18 | FDA UDI | Class II | Active |
| Extra Articular Distal Humerus Plate | MDS170108L | FDA UDI | Class II | Active |
| 2.0mm Drill | MDS101120165 | FDA UDI | Class II | Active |
| Distal Radius Plating System Case Lid | MDS141202 | FDA UDI | Class II | Active |
| Broad Plate, 3.5T | MDS1101B20 | FDA UDI | Class II | Active |
| Drill Guide for 2.7mm and 2.0mm Drill | MDS110821 | FDA UDI | Class II | Active |
| Injection Screw, Ø3.5mm | MDS1102IN57 | FDA UDI | Class II | Active |
| Proximal Humerus Plate | MDS130111R | FDA UDI | Class II | Active |
| Cortical Screw, 2.0mm | MDS1902X16 | FDA UDI | Class II | Active |
| Cortical Screw, 2.7mm | MDS1002X48 | FDA UDI | Class II | Active |
| K-Wire, Ø1.1 x 120mm | MDS001011120R | FDA UDI | Class II | Active |
| Distal Humerus Plate, Posterolateral | MDS170105LP | FDA UDI | Class II | Active |
| Injection Screw, Ø3.5mm | MDS1102IN42 | FDA UDI | Class II | Active |
| K-Wire Depth Gauge | MDS100702 | FDA UDI | Class II | Active |
| Cortical Screw, 2.7mm | MDS1002X38 | FDA UDI | Class II | Active |
| Extra Articular Distal Humerus Plate | MDS170108R | FDA UDI | Class II | Active |
| Drill Guide Block Narrow, Left | MDS140907L | FDA UDI | Class II | Active |
| Broad Plate, 3.5T | MDS1101B05 | FDA UDI | Class II | Active |
| Multiuse Screw, 3.5mm | MDS1102M30 | FDA UDI | Class II | Active |
| 2.0 Cannulated Drill | MDS101120165C | FDA UDI | Class II | Active |
| Torque Limiter Ball Handle | MDS000608AOT | FDA UDI | Class II | Active |
| Multiuse Screw, 3.5mm | MDS1102M42 | FDA UDI | Class II | Active |
| Proximal Humerus Plating System Case Lid | MDS131202 | FDA UDI | Class II | Active |
| Low Profile Head Screw, 2.7mm | MDS1002CO36 | FDA UDI | Class II | Active |
| Broad Plate, 3.5T | MDS1101B22 | FDA UDI | Class II | Active |
Related Companies
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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.
The FDA recall records for Miami Device Solutions show 1 recall record. This recall was initiated on 2019-01-15 and its status is recorded as terminated. The reason given for the recall is related to Right Proximal Humerus Plates, specifically that product component parts MDS130108R may be improperly identified as left.
AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Jan 15, 2019 | Z-0603-2020 | — | terminated | Right Proximal Humerus Plates. Product component parts MDS130108R, may be improperly identified as left. |