Pioneer Surgical Technology, Inc. (contract manufacturer, Marquette, MI): 9 new FDA device listings, incl. cerclage, fixation
Pioneer Surgical Technology, Inc. (Marquette, Michigan): 9 new FDA device listings, incl. cerclage, fixation. Its amount of 9 is top-decile (92nd percentile of 2,570 records). Dated 86 days ago, it serves as a historical benchmark. Score 80/100. As of 2026-10-28, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).
Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
amount: 9 · 92th percentile of 2,570 DeviceEstablishmentPulse records · 9.0x the median
Free preview: all 14 published fields of this record are shown below. Locked: 24 related MI DeviceEstablishmentPulse records and the 5-column CSV export.
| 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 |
| amount percentile | 92th of 2,570 (median 1, 9.0x median) |
| Peer records CSV (25 MI records) | 🔒 Click to unlock → |
| CRM-ready export with official source URLs | 🔒 Click to unlock → |
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL
- Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
- Record date: 2026-08-10
- Data refreshed: 2026-10-28
- Refunds on request within 14 days
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LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 28 Oct 2026 20:51:27 GMT
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Peer benchmark and outreach value: Pioneer Surgical Technology, Inc. and 25 Michigan peers
- Michigan DeviceEstablishmentPulse records like this one: 25
- Pioneer Surgical Technology, Inc.'s amount: 92nd percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Michigan peer: $5,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
80 / 100 Score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.
What is the DeviceEstablishmentPulse record for Pioneer Surgical Technology, Inc. in Marquette, Michigan?
Pioneer Surgical Technology, Inc. (Marquette, MI), a contract manufacturer, added 9 FDA device listings between 2026-06-19 and 2026-08-10.
How does Pioneer Surgical Technology, Inc. compare to other Michigan DeviceEstablishmentPulse records?
This is a top-decile record: its amount of 9 is 9.0x the median of 1 across 2,570 records. It is 86 days old; check the official source for later updates before acting. Its Score of 80/100 puts it among the stronger signals in this feed.
Pioneer Surgical Technology, Inc. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Pioneer Surgical Technology, Inc. | Marquette, MI | 9 | 92nd | 2026-08-10 |
| Arthrex, Inc. | Ave Maria, FL | 10 | 93rd | 2026-09-27 |
| Biopro, Inc. | Port Huron, MI | 11 | 94th | 2026-10-15 |
| NGInstruments, Inc dba Avalign Cutting Instruments | Warsaw, IN | 4 | 83rd | 2026-10-16 |
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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.