Apothecaries Sundries Mfg Pvt Ltd (manufacturer, GURUGRAM Haryana, IN): 26 new FDA device listings, incl. shoe, cast

Apothecaries Sundries Mfg Pvt Ltd (GURUGRAM Haryana, Indiana): 26 new FDA device listings, incl. shoe, cast. Its amount of 26 is top-decile (98th percentile of 2,570 records). Dated 133 days ago, it serves as a historical benchmark. Score 75/100. 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: 26 · 98th percentile of 2,570 DeviceEstablishmentPulse records · 26.0x the median

Free preview: all 14 published fields of this record are shown below. Locked: 72 related IN DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentApothecaries Sundries Mfg Pvt Ltd
RoleManufacturer
Establishment typesRepack or Relabel Medical Device; Manufacture Medical Device
LocationGURUGRAM Haryana, IN
New listings26
DevicesShoe, Cast; Binder, Abdominal; Assembly, Thigh/Knee/Shank/Ankle/Foot, External; Attachment, Commode, Wheelchair; Binder, Elastic; Bag, Ice; Assembly, Knee/Shank/Ankle/Foot, External; Orthosis, Rib Fracture, Soft; Orthosis, Cervical; Orthosis, Cervical-Thoracic, Rigid
Product codesIPG, FSD, KFX, INB, KMO, KYR, ISW, IPX, IQK, IQF, IQJ, INP, KFT, KTD, ITJ
Device classesClass I, Class II
Medical specialtiesPhysical Medicine, General Hospital
Brand namesComfoSmart; Abdominal Splint; Brace, Splint, Immobilizer; Commode Stool, Chair, Wheelchair; Ankle Wrap with binder; Elastic Ankle Binder; Elastic Tubular Anklet with Binder; Ankle Brace
First new listing2026-05-23
Latest new listing2026-06-25
FDA registration number3007123908
Registration expires2026-12-31
amount percentile98th of 2,570 (median 1, 26.0x 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: 2026-06-25
  • 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: Apothecaries Sundries Mfg Pvt Ltd and 73 Indiana peers

  • Indiana DeviceEstablishmentPulse records like this one: 73
  • Apothecaries Sundries Mfg Pvt Ltd's amount: 98th 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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75 / 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.

What is the DeviceEstablishmentPulse record for Apothecaries Sundries Mfg Pvt Ltd in GURUGRAM Haryana, Indiana?

Apothecaries Sundries Mfg Pvt Ltd (GURUGRAM Haryana, IN), a manufacturer, added 26 FDA device listings between 2026-05-23 and 2026-06-25.

How does Apothecaries Sundries Mfg Pvt Ltd compare to other Indiana DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 26 is 26.0x the median of 1 across 2,570 records. It is 133 days old; check the official source for later updates before acting. Its Score of 75/100 puts it among the stronger signals in this feed.

Apothecaries Sundries Mfg Pvt Ltd vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Apothecaries Sundries Mfg Pvt LtdGURUGRAM Haryana, IN2698th2026-06-25
Boston Scientific CorporationSaint Paul, MN2498th2026-10-16
Ge Parallel Design, Inc.Phoenix, AZ1997th2026-10-07
Surgentec LLCBoca Raton, FL1596th2026-10-16

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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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