# Pioneer Surgical Technology, Inc. (contract manufacturer, Marquette, MI): 9 new FDA device listings, incl. cerclage, fixation

**Score:** 80/100

| Field | Value |
|---|---|
| Establishment | Pioneer Surgical Technology, Inc. |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device; Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Marquette, MI, US |
| New listings | 9 |
| Devices | Cerclage, Fixation; Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component; Screw, Fixation, Bone; Washer, Bolt Nut; Plate, Fixation, Bone; Intervertebral Fusion Device With Integrated Fixation, Lumbar |
| Product codes | JDQ, KTT, HWC, HTN, HRS, OVD |
| Device classes | Class II |
| Medical specialties | Orthopedic |
| Brand names | Cable-Ready® Cable Grip System; VOLT™ Medial Distal Femur Plate 3.5; VOLT™ Ankle Trauma 2.7/3.5 Plating System; VOLT™ Calcaneus 2.7 Plating System |
| First new listing | 2026-06-19 |
| Latest new listing | 2026-08-10 |
| FDA registration number | 1833824 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.