Laparomed Private Limited (manufacturer, Mumbai Maharashtra, IN): 51 new FDA device listings, incl. probe, periodontic

Laparomed Private Limited (Mumbai Maharashtra, Indiana): 51 new FDA device listings, incl. probe, periodontic. Its amount of 51 is top-decile (99th percentile of 2,570 records). Dated 183 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: 51 · 99th percentile of 2,570 DeviceEstablishmentPulse records · 51.0x 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
EstablishmentLaparomed Private Limited
Owner / operatorLaparo Med Private Limited
RoleManufacturer
Establishment typesManufacture Medical Device
LocationMumbai Maharashtra, IN
New listings51
DevicesProbe, Periodontic; Spatula, Surgical, General & Plastic Surgery; Mirror, Mouth; Retractor; Handle, Scalpel; Retractor, Ophthalmic; Control, Platelet; Holder, Needle; Orthopedic; Gag, Mouth; Forceps, Ophthalmic
Product codesEIX, GAF, EAX, GAD, GDZ, HNI, GJP, HXK, KBN, HNR, HTD, EBH, FWF, EMJ, EKJ
Device classesClass I, Class II
Medical specialtiesDental, General, Plastic Surgery, Ophthalmic, Hematology, Orthopedic, Ear, Nose, Throat, Gastroenterology, Urology, Obstetrics/Gynecology, Neurology, General Hospital
Brand namesEXPLORERS & PROBES; CEMENT SPATULAS, LAPAROSCOPIC SPATULA; MOUTH MIRROR AND HANDLES; REATRACTORS (NON-SURGICAL), RETRACTOR, LAPAROSCOPIC FAN RETRACTOR; SCALPELS; OPTHALMIC RETRACTORS; ARTICULATORS; NEEDLE HOLDER
First new listing2026-05-05
Latest new listing2026-05-05
FDA registration number3045853999
Registration expires2026-12-31
amount percentile99th of 2,570 (median 1, 51.0x 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: 2026-05-05
  • 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: Laparomed Private Limited and 73 Indiana peers

  • Indiana DeviceEstablishmentPulse records like this one: 73
  • Laparomed Private Limited'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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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 Laparomed Private Limited in Mumbai Maharashtra, Indiana?

Laparomed Private Limited (Mumbai Maharashtra, IN), a manufacturer, added 51 FDA device listings on 2026-05-05.

How does Laparomed Private Limited compare to other Indiana DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 51 is 51.0x the median of 1 across 2,570 records. It is 183 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.

Laparomed Private Limited vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Laparomed Private LimitedMumbai Maharashtra, IN5199th2026-05-05
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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✓ Read-only, live public data · Key and unlock right after payment · Card, Apple Pay, Google Pay or Link via Stripe · Refunds on request within 14 days

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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