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

Biopro, Inc. (Port Huron, Michigan): 11 new FDA device listings, incl. system, skin closure. Its amount of 11 is top-decile (94th percentile of 2,570 records). Dated 20 days ago, it is in the active follow-up window. Score 90/100. 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: 11 · 94th percentile of 2,570 DeviceEstablishmentPulse records · 11.0x 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.

FieldValue
EstablishmentBiopro, Inc.
RoleContract manufacturer
Establishment typesManufacture Medical Device for Another Party (Contract Manufacturer); Repack or Relabel Medical Device
LocationPort Huron, MI, US
New listings11
DevicesSystem, 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 codesMKY, GAD, KWY, MEH, OQG, LPH, OQI, LZO, MAX, HAW
Device classesClass I, Class II
Medical specialtiesGeneral, Plastic Surgery, Orthopedic, Neurology
Brand namesQuikZip 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 listing2026-05-06
Latest new listing2026-10-15
FDA registration number1833506
Registration expires2027-12-31
amount percentile94th of 2,570 (median 1, 11.0x median)
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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: 2026-10-15
  • 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: Biopro, Inc. and 25 Michigan peers

  • Michigan DeviceEstablishmentPulse records like this one: 25
  • Biopro, Inc.'s amount: 94th percentile of 2,570 records
  • Timing: Medium: dated in the last 30 days
  • Estimated pipeline if you contact every Michigan peer: $5,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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90 / 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.
  • Listed in the last 45 days.

What is the DeviceEstablishmentPulse record for Biopro, Inc. in Port Huron, Michigan?

Biopro, Inc. (Port Huron, MI), a contract manufacturer, added 11 FDA device listings between 2026-05-06 and 2026-10-15.

How does Biopro, Inc. compare to other Michigan DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 11 is 11.0x the median of 1 across 2,570 records. It is 20 days old, still within a typical 45-day follow-up window. Its Score of 90/100 puts it among the stronger signals in this feed.

Biopro, Inc. vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Biopro, Inc.Port Huron, MI1194th2026-10-15
Arthrex, Inc.Ave Maria, FL1093rd2026-09-27
Arthrex Manufacturing Inc.Pendleton, SC790th2026-09-27
NGInstruments, Inc dba Avalign Cutting InstrumentsWarsaw, IN483rd2026-10-16

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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.

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