Viant AS&O Holdings, LLC (contract manufacturer, Indianapolis, IN): 4 new FDA device listings, incl. sterilization wrap containers, trays, cassettes & other accessories

Viant AS&O Holdings, LLC (Indianapolis, Indiana): 4 new FDA device listings, incl. sterilization wrap containers, trays, cassettes & other accessories. Its amount of 4 is above the median of 1 (83rd percentile). Dated 78 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: 4 · 83th percentile of 2,570 DeviceEstablishmentPulse records · 4.0x 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
EstablishmentViant AS&O Holdings, LLC
Owner / operatorViant Medical, LLC
RoleContract manufacturer
Establishment typesManufacture Medical Device for Another Party (Contract Manufacturer)
LocationIndianapolis, IN, US
New listings4
DevicesSterilization Wrap Containers, Trays, Cassettes & Other Accessories; Appliance, Fixation, Spinal Intervertebral Body; Appliance, Fixation, Spinal Interlaminal
Product codesKCT, KWQ, KWP
Device classesClass II
Medical specialtiesGeneral Hospital, Orthopedic
Brand namesBASE, OUTER 2.5 INCH DEEP; CD Horizon® Implant Tray and Instruments; SHILLA Instrument Tray 2 - Case 3; Dual Lead Tap Tray; SHILLA 5.5 Instrument Tray 1 - Case 5; CASE, MRC IMPLANT, TI; SHILLA 5.5 Instrument Tray 1 - Case 3; TRAY,6970118,PRESTIGELP OUS INSERTR&6X18
First new listing2026-08-04
Latest new listing2026-08-19
FDA registration number1832228
Registration expires2026-12-31
amount percentile83th of 2,570 (median 1, 4.0x 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: 2026-08-19
  • 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: Viant AS&O Holdings, LLC and 73 Indiana peers

  • Indiana DeviceEstablishmentPulse records like this one: 73
  • Viant AS&O Holdings, LLC's amount: 83rd 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 Viant AS&O Holdings, LLC in Indianapolis, Indiana?

Viant AS&O Holdings, LLC (Indianapolis, IN), a contract manufacturer, added 4 FDA device listings between 2026-08-04 and 2026-08-19.

How does Viant AS&O Holdings, LLC compare to other Indiana DeviceEstablishmentPulse records?

Its amount of 4 sits in the upper half (83th percentile) of 2,570 records; the median is 1. It is 78 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.

Viant AS&O Holdings, LLC vs. top 3 peers

OrganizationLocationAmountPercentileRecord dateCompare
Viant AS&O Holdings, LLCIndianapolis, IN483rd2026-08-19This record
NGInstruments, Inc dba Avalign Cutting InstrumentsWarsaw, IN483rd2026-10-16Compare Viant AS&O Holdings, LLC vs NGInstruments, Inc dba Avalign Cutting Instruments →
Cook Medical LLCBloomington, IN483rd2026-10-13Compare Viant AS&O Holdings, LLC vs Cook Medical LLC →
Zimmer, Inc.Warsaw, IN2898th2026-09-29View record →

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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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