Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3039406055

FEI Number

3039406055

Entity Name

INTERNATIONAL PRECISION MOLDS

City/State/Country

COYOL Alajuela, CR

Establishment Address

1.5 km south, 1.5 km west from Dekra, Condominio Industrial Indupark, Coyol, COYOL Alajuela 20102, CR

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

International Precision Molds (Owner Number: 10093655)

Owner / Operator Contact Address

1.5 km south, 1.5 km west from Dekra, Condominio Industrial Indupark, Coyol, COYOL, CR-A 20102, CR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KDD	Kit, Surgical Instrument, Disposable	General, Plastic Surgery	Class 1	878.4800	2025-06-17
GDI	Dissector, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2025-06-17

Official Correspondent

Nelson Cruz

US Agent Details

Bill Jacqmein Email: bjacqmein@primepathmedtech.com Phone: (404) 2166190

Related Public Records

Same Entity

International Precision Molds

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3039406055. Last updated year: 2026. Please use registration number 3039406055 when referencing this establishment in official correspondence.