# Biopro, Inc. (contract manufacturer, Port Huron, MI): 11 new FDA device listings, incl. system, skin closure

**Score:** 90/100

| Field | Value |
|---|---|
| Establishment | Biopro, Inc. |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer); Repack or Relabel Medical Device |
| Location | Port Huron, MI, US |
| New listings | 11 |
| Devices | System, Skin Closure; Retractor; Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented; Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate; Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented; Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented; Hip, Semi-Constrained, Cemented, Metal/Ceramic/Polymer + Additive, Porous Uncemented; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented; Intervertebral Fusion Device With Bone Graft, Lumbar; Neurological Stereotaxic Instrument |
| Product codes | MKY, GAD, KWY, MEH, OQG, LPH, OQI, LZO, MAX, HAW |
| Device classes | Class I, Class II |
| Medical specialties | General, Plastic Surgery, Orthopedic, Neurology |
| Brand names | QuikZip Wound Closure Device; Hintermann Compressor; Hintermann Distractor; TheRay Collared and Collarless Hip System; Logic Titanium Interbody Fusion System; Radix Lens; Libertas Bipolar Head |
| First new listing | 2026-05-06 |
| Latest new listing | 2026-10-15 |
| FDA registration number | 1833506 |
| Registration expires | 2027-12-31 |

## 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.
- Listed in the last 45 days.

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.