Micropulse Inc (contract manufacturer, Columbia City, IN): 45 new FDA device listings, incl. intervertebral fusion device with integrated fixation, lumbar

Micropulse Inc (Columbia City, Indiana): 45 new FDA device listings, incl. intervertebral fusion device with integrated fixation, lumbar. Its amount of 45 is top-decile (99th percentile of 2,570 records). Dated 76 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: 45 · 99th percentile of 2,570 DeviceEstablishmentPulse records · 45.0x the median

Free preview: all 15 published fields of this record are shown below. Locked: 72 related IN DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentMicropulse Inc
Owner / operatorMicropulse
RoleContract manufacturer
Establishment typesManufacture Medical Device for Another Party (Contract Manufacturer)
LocationColumbia City, IN, US
New listings45
DevicesIntervertebral Fusion Device With Integrated Fixation, Lumbar; Intervertebral Fusion Device With Bone Graft, Lumbar; Intervertebral Fusion Device With Bone Graft, Thoracic; Intervertebral Fusion Device With Bone Graft, Cervical; Appliance, Fixation, Spinal Intervertebral Body; Spinal Vertebral Body Replacement Device - Cervical; Spinal Vertebral Body Replacement Device; Intervertebral Fusion Device With Integrated Fixation, Cervical
Product codesOVD, MAX, PHM, ODP, KWQ, PLR, MQP, OVE
Device classesClass II
Medical specialtiesOrthopedic
Brand namesAMP II; IdentiTi ll; IdentiTi; Segmental Plating System; Proximity; Transcend; Calibrate; AMP-LTX
First new listing2026-08-20
Latest new listing2026-08-20
FDA registration number1834379
Registration expires2026-12-31
amount percentile99th of 2,570 (median 1, 45.0x 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: 2026-08-20
  • 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: Micropulse Inc and 73 Indiana peers

  • Indiana DeviceEstablishmentPulse records like this one: 73
  • Micropulse Inc's amount: 99th percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every Indiana peer: $14,600 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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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 Micropulse Inc in Columbia City, Indiana?

Micropulse Inc (Columbia City, IN), a contract manufacturer, added 45 FDA device listings on 2026-08-20.

How does Micropulse Inc compare to other Indiana DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 45 is 45.0x the median of 1 across 2,570 records. It is 76 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.

Micropulse Inc vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Micropulse IncColumbia City, IN4599th2026-08-20
Zimmer, Inc.Warsaw, IN2898th2026-09-29
NGInstruments, Inc dba Avalign Cutting InstrumentsWarsaw, IN483rd2026-10-16
Cook Medical LLCBloomington, IN483rd2026-10-13

Related records

DeviceEstablishmentPulse: Contract manufacturer DeviceEstablishmentPulse: U.S. establishment DeviceEstablishmentPulse: records in Indiana

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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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