Surgicon Pvt Ltd (contract manufacturer, Sialkot Punjab, PK): 9 new FDA device listings, incl. pick, microsurgical ear

Surgicon Pvt Ltd (Sialkot Punjab): 9 new FDA device listings, incl. pick, microsurgical ear. Its amount of 9 is top-decile (92nd percentile of 2,709 records). Dated 48 days ago, it serves as a historical benchmark. Score 55/100. As of 2026-11-04, 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: 9 · 92th percentile of 2,709 DeviceEstablishmentPulse records · 4.5x the median

Free preview: all 14 published fields of this record are shown below. Locked: 12 related PK DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentSurgicon Pvt Ltd
RoleContract manufacturer
Establishment typesManufacture Medical Device for Another Party (Contract Manufacturer); Remanufacture Medical Device; Manufacture Medical Device
LocationSialkot Punjab, PK
New listings9
DevicesPick, Microsurgical Ear; Tape, Measuring, Rulers And Calipers; Excavator, Ear; Trocar, Ent; Probe, Ent; Block, Cutting, Ent, Non-Sterile; Hook, Microsurgical Ear; Mobilizer, Ent; Stripper, Surgical
Product codesJYT, FTY, JYH, KTE, KAK, NNR, JYL, KAJ, HRT
Device classesClass I
Medical specialtiesEar, Nose, Throat, General, Plastic Surgery, Orthopedic
Brand namesPICK, MICROSURGICAL EAR; TAPE, MEASURING, RULERS AND CALIPERS; EXCAVATOR, EAR; TROCAR; PROBE, ENT; BLOCK, CUTTING, ENT; HOOK, MICROSURGICAL EAR; MOBILIZER, ENT
First new listing2026-09-18
Latest new listing2026-09-18
FDA registration number3007597038
Registration expires2026-12-31
amount percentile92th of 2,709 (median 2, 4.5x 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: 2026-09-18
  • Data refreshed: 2026-11-04
  • Refunds on request within 14 days

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Top DeviceEstablishmentPulse records (PK first): Acheron Instruments (Pvt.) Ltd. (manufacturer, LAHORE Punjab · Medcave Private Limited (manufacturer, Sialkot Punjab, PK) · Hexamed Pvt Ltd (contract manufacturer, Sialkot Punjab, PK) · Densol International (Private) Limited (manufacturer, Sialko · Acme Commercial Ways Ltd. (manufacturer, Sialkot Punjab, PK) · Browse all by state and category →

LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 04 Nov 2026 21:52:36 GMT

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Peer benchmark and outreach value: Surgicon Pvt Ltd and 13 PK peers

  • PK DeviceEstablishmentPulse records like this one: 13
  • Surgicon Pvt Ltd's amount: 92nd percentile of 2,709 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every PK peer: $2,600 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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55 / 100 Score

  • Contract manufacturer or sterilizer adding work.
  • Several new listings at once.

What is the DeviceEstablishmentPulse record for Surgicon Pvt Ltd in Sialkot Punjab?

Surgicon Pvt Ltd (Sialkot Punjab, PK), a contract manufacturer, added 9 FDA device listings on 2026-09-18.

How does Surgicon Pvt Ltd compare to other DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 9 is 4.5x the median of 2 across 2,709 records. It is 48 days old; check the official source for later updates before acting.

Surgicon Pvt Ltd vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Surgicon Pvt LtdSialkot Punjab, PK992nd2026-09-18
Biopro, Inc.Port Huron, MI1092nd2026-10-15
NGInstruments, Inc dba Avalign Cutting InstrumentsWarsaw, IN483rd2026-10-16
Cook Medical LLCBloomington, IN483rd2026-10-13

Related records

DeviceEstablishmentPulse: Contract manufacturer DeviceEstablishmentPulse: Foreign establishment

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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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