Wipro Ge Medical Device Manufacturing Private Limited (manufacturer, Bangalore Karnataka, IN): 19 new FDA device listings, incl. system, imaging, pulsed doppler, ultrasonic

Wipro Ge Medical Device Manufacturing Private Limited (Bangalore Karnataka, Indiana): 19 new FDA device listings, incl. system, imaging, pulsed doppler, ultrasonic. Its amount of 19 is top-decile (97th percentile of 2,570 records). Dated 28 days ago, it is in the active follow-up window. Score 85/100. 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: 19 · 97th percentile of 2,570 DeviceEstablishmentPulse records · 19.0x 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
EstablishmentWipro Ge Medical Device Manufacturing Private Limited
Owner / operatorGE HealthCare Technologies Inc.
RoleManufacturer
Establishment typesManufacture Medical Device
LocationBangalore Karnataka, IN
New listings19
DevicesSystem, Imaging, Pulsed Doppler, Ultrasonic; System, Imaging, Pulsed Echo, Ultrasonic; Transducer, Ultrasonic, Diagnostic; Automated Radiological Image Processing Software; Twister, Brace Setting
Product codesIYN, IYO, ITX, QIH, ITO
Device classesClass I, Class II
Medical specialtiesRadiology, Physical Medicine
Brand namesL4-20t-RS; 4C-RS; P6D; 6Tc-RS; 9L-RS; RAB2-6-RS; LOGIQ Focus; 3Sc-RS
First new listing2026-06-01
Latest new listing2026-10-07
FDA registration number3032109181
Registration expires2027-12-31
amount percentile97th of 2,570 (median 1, 19.0x 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: 2026-10-07
  • 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: Wipro Ge Medical Device Manufacturing Private Limited and 73 Indiana peers

  • Indiana DeviceEstablishmentPulse records like this one: 73
  • Wipro Ge Medical Device Manufacturing Private Limited's amount: 97th percentile of 2,570 records
  • Timing: Medium: dated in the last 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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85 / 100 Score

  • Brings its own devices to market: buys manufacturing, sterilization and QMS help.
  • Class II or III devices: QMS and regulatory demands.
  • Several new listings at once.
  • Listed in the last 45 days.

What is the DeviceEstablishmentPulse record for Wipro Ge Medical Device Manufacturing Private Limited in Bangalore Karnataka, Indiana?

Wipro Ge Medical Device Manufacturing Private Limited (Bangalore Karnataka, IN), a manufacturer, added 19 FDA device listings between 2026-06-01 and 2026-10-07.

How does Wipro Ge Medical Device Manufacturing Private Limited compare to other Indiana DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 19 is 19.0x the median of 1 across 2,570 records. It is 28 days old, still within a typical 45-day follow-up window. Its Score of 85/100 puts it among the stronger signals in this feed.

Wipro Ge Medical Device Manufacturing Private Limited vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Wipro Ge Medical Device Manufacturing Private LimitedBangalore Karnataka, IN1997th2026-10-07
Ge Parallel Design, Inc.Phoenix, AZ1997th2026-10-07
Surgentec LLCBoca Raton, FL1596th2026-10-16
Boston Scientific CorporationSaint Paul, MN2498th2026-10-16

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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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