[DeviceEstablishmentPulse](/v/deviceestablishmentpulse) / compare

# Biopro, Inc. vs Packaging Compliance Medical, LLC: DeviceEstablishmentPulse comparison

**Biopro, Inc.'s new listings of 10 is 1.0x Packaging Compliance Medical, LLC's 10 (92nd percentile). Biopro, Inc. is dated 2026-10-15; Packaging Compliance Medical, LLC 2026-05-27.**

Data as of 2026-11-04 · [Compiled by Zalwin](/research/deviceestablishmentpulse) from openFDA device registration and listing endpoint (U.S. Food and Drug Administration) Copy citation

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## How does Biopro, Inc. compare to Packaging Compliance Medical, LLC?

| Field | Biopro, Inc. | Packaging Compliance Medical, LLC |
|---|---|---|
| Establishment | Biopro, Inc. | Packaging Compliance Medical, LLC |
| Role | Contract manufacturer | Contract manufacturer |
| Establishment types | Repack or Relabel Medical Device; Manufacture Medical Device for Another Party (Contract Manufacturer) | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Port Huron, MI, US | Kentwood, MI, US |
| New listings | 10 | 10 |
| Devices | Neurological Stereotaxic Instrument; Intervertebral Fusion Device With Bone Graft, Lumbar; System, Skin Closure; 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 | Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment; Reamer; Hammer, Surgical; Extractor; Bit, Drill; Bit, Surgical; Guide, Surgical, Instrument; Driver, Surgical, Pin; Plate, Fixation, Bone; Punch, Surgical |
| Product codes | HAW, MAX, MKY, KWY, MEH, OQG, LPH, OQI, LZO | KIJ, HTO, FZY, HWB, HTW, GFG, FZX, GFC, HRS, LRY |
| Device classes | Class I, Class II | Class I, Class II |
| Medical specialties | Neurology, Orthopedic, General, Plastic Surgery | General, Plastic Surgery, Orthopedic |
| Brand names | Radix Lens; Logic Titanium Interbody Fusion System; QuikZip Wound Closure Device; Libertas Bipolar Head; TheRay Collared and Collarless Hip System | 3.2mm x 330mm K-Wire, Threaded, 316L; Conical Reamer, 9.75mm, Long; Conical Reamer, 11mm, Short; Conical Reamer, 11mm, Long; Conical Reamer, 9.75mm, Short; 10mm Opening Reamer; 12mm Opening Reamer; 7.5/9.5 STEPPED ENTRY REAMER |
| First new listing | 2026-10-15 | 2026-05-27 |
| Latest new listing | 2026-10-15 | 2026-05-27 |
| FDA registration number | 1833506 | 3014967969 |
| Registration expires | 2027-12-31 | 2027-12-31 |
| amount percentile | 92nd | 92nd |
| Score | 90/100 | 80/100 |
| Peer rank and all 27 MI records (CSV) | Every comparable record ranked, with amounts, dates and scores 🔒 Click to unlock → |
| Official source URLs for every peer record | Direct links to each record at its government source 🔒 Click to unlock → |

Official records: [Biopro, Inc.](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm) · [Packaging Compliance Medical, LLC](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm)

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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.

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