Millstone Medical Outsourcing LLC. (contract manufacturer, Fall River, MA): 24 new FDA device listings, incl. peripheral blood processing device for wound management

Millstone Medical Outsourcing LLC. (Fall River, Massachusetts): 24 new FDA device listings, incl. peripheral blood processing device for wound management. Its amount of 24 is top-decile (98th percentile of 2,570 records). Dated 27 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: 24 · 98th percentile of 2,570 DeviceEstablishmentPulse records · 24.0x the median

Free preview: all 14 published fields of this record are shown below. Locked: 69 related MA DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentMillstone Medical Outsourcing LLC.
RoleContract manufacturer
Establishment typesManufacture Medical Device for Another Party (Contract Manufacturer)
LocationFall River, MA, US
New listings24
DevicesPeripheral Blood Processing Device For Wound Management; Thoracolumbosacral Pedicle Screw System; Needle, Suturing, Disposable; Orthopedic Augmented Reality; Orthopedic Stereotaxic Instrument; Intervertebral Fusion Device With Bone Graft, Cervical; Shoulder Prosthesis, Reverse Configuration; Intervertebral Fusion Device With Bone Graft, Thoracic; Intervertebral Fusion Device With Integrated Fixation, Lumbar; Intervertebral Fusion Device With Bone Graft, Lumbar
Product codesPMQ, NKB, GAB, SBF, OLO, ODP, PHX, PHM, OVD, MAX, JWH, OVE
Device classesClass I, Class II
Medical specialtiesHematology, Orthopedic, General, Plastic Surgery, Neurology
Brand namesROSA® Shoulder System
First new listing2026-05-29
Latest new listing2026-10-08
FDA registration number1226544
Registration expires2027-12-31
amount percentile98th of 2,570 (median 1, 24.0x 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: 2026-10-08
  • 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: Millstone Medical Outsourcing LLC. and 70 Massachusetts peers

  • Massachusetts DeviceEstablishmentPulse records like this one: 70
  • Millstone Medical Outsourcing LLC.'s amount: 98th percentile of 2,570 records
  • Timing: Medium: dated in the last 30 days
  • Estimated pipeline if you contact every Massachusetts peer: $14,000 (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 Millstone Medical Outsourcing LLC. in Fall River, Massachusetts?

Millstone Medical Outsourcing LLC. (Fall River, MA), a contract manufacturer, added 24 FDA device listings between 2026-05-29 and 2026-10-08.

How does Millstone Medical Outsourcing LLC. compare to other Massachusetts DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 24 is 24.0x the median of 1 across 2,570 records. It is 27 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.

Millstone Medical Outsourcing LLC. vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Millstone Medical Outsourcing LLC.Fall River, MA2498th2026-10-08
Zimmer, Inc.Warsaw, IN2898th2026-09-29
Philips Ultrasound LLCReedsville, PA3298th2026-09-30
Biopro, Inc.Port Huron, MI1194th2026-10-15

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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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