HARMAC MEDICAL PRODUCTS, INC./H3 de Tijuana, S. de RL de C.V. (contract manufacturer, Tijuana Baja California, MX): 27 new FDA device listings, incl. unit, phacofragmentation

HARMAC MEDICAL PRODUCTS, INC./H3 de Tijuana, S. de RL de C.V. (Tijuana Baja California): 27 new FDA device listings, incl. unit, phacofragmentation. Its amount of 27 is top-decile (98th percentile of 2,709 records). Dated 162 days ago, it serves as a historical benchmark. Score 70/100. 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: 27 · 98th percentile of 2,709 DeviceEstablishmentPulse records · 13.5x the median

Free preview: all 14 published fields of this record are shown below. Locked: 7 related MX DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentHARMAC MEDICAL PRODUCTS, INC./H3 de Tijuana, S. de RL de C.V.
Owner / operatorHarmac Medical Products, Inc.
RoleContract manufacturer
Establishment typesManufacture Medical Device for Another Party (Contract Manufacturer)
LocationTijuana Baja California, MX
New listings27
DevicesUnit, Phacofragmentation; Endoilluminator; Cannula, Trocar, Ophthalmic; Cannula, Ophthalmic; Media, Corneal Storage; Apparatus, Cautery, Radiofrequency, Ac-Powered; Instrument, Vitreous Aspiration And Cutting, Ac-Powered; Photocoagulator And Accessories; Laser, Ophthalmic; Knife, Ophthalmic
Product codesHQC, MPA, NGY, HMX, LYX, HQR, HQE, HQB, HQF, HNN, HOY, MDM, GZX, KKX
Device classesClass I, Class II, Unclassified
Medical specialtiesOphthalmic, Gastroenterology, Urology, General, Plastic Surgery, Neurology
First new listing2026-05-08
Latest new listing2026-05-27
FDA registration number3045817901
Registration expires2027-12-31
amount percentile98th of 2,709 (median 2, 13.5x 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: 2026-05-27
  • Data refreshed: 2026-11-04
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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: HARMAC MEDICAL PRODUCTS, INC./H3 de Tijuana, S. de RL de C.V. and 8 MX peers

  • MX DeviceEstablishmentPulse records like this one: 8
  • HARMAC MEDICAL PRODUCTS, INC./H3 de Tijuana, S. de RL de C.V.'s amount: 98th percentile of 2,709 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every MX peer: $1,600 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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70 / 100 Score

  • Contract manufacturer or sterilizer adding work.
  • Class II or III devices: QMS and regulatory demands.
  • Several new listings at once.

What is the DeviceEstablishmentPulse record for HARMAC MEDICAL PRODUCTS, INC./H3 de Tijuana, S. de RL de C.V. in Tijuana Baja California?

HARMAC MEDICAL PRODUCTS, INC./H3 de Tijuana, S. de RL de C.V. (Tijuana Baja California, MX), a contract manufacturer, added 27 FDA device listings between 2026-05-08 and 2026-05-27.

How does HARMAC MEDICAL PRODUCTS, INC./H3 de Tijuana, S. de RL de C.V. compare to other DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 27 is 13.5x the median of 2 across 2,709 records. It is 162 days old; check the official source for later updates before acting. Its Score of 70/100 puts it among the stronger signals in this feed.

HARMAC MEDICAL PRODUCTS, INC./H3 de Tijuana, S. de RL de C.V. vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
HARMAC MEDICAL PRODUCTS, INC./H3 de Tijuana, S. de RL de C.V.Tijuana Baja California, MX2798th2026-05-27
Zimmer, Inc.Warsaw, IN2898th2026-09-29
Millstone Medical Outsourcing LLC.Fall River, MA2497th2026-10-08
Philips Ultrasound LLCReedsville, PA3298th2026-09-30

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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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