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Data / Medical devices / Mexico / Internacional Farmaceutica, S.A. De C.V.

Internacional Farmaceutica, S.A. De C.V.: FDA-registered device maker in Mexico City, Mexico, 10 510(k) clearances

Internacional Farmaceutica, S.A. De C.V. is registered with the FDA (registration 1000274611) in Mexico City, Mexico. It lists 8 device types. The FDA files 10 510(k) clearances under its listings, the newest dated May 23, 2008. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
1000274611
Address
Carreteraco No. 44 Colonia Parque San Andres Coyoacan, Mexico City, Mexico, 04040
Owner or operator
INTERNACIONAL FARMACEUTICA, S.A. DE C.V. (9051246)
Roles
Manufacturer
First device listed
July 15, 2005
Registered through
2026
Brand names listed
Atramat CHROMIC GUT, Atramat NYLON, Atramat PDX, Atramat PGA, Atramat PGA RAPID, Atramat PGC25, Atramat PGLA90, Atramat PLAIN GUT and more

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
May 23, 2008K072863ATRAMAT PGC25 POLY(GLYCOLIDE-CO-EPSILON-CAPROLACTONE) SURGICAL SUTURESGAMSubstantially EquivalentInternacional Farmaceutica, S.A. DE C.V.accessdata.fda.gov
May 23, 2008K072859ATRAMAT PGLA90 POLY(GLYCOLIDE-CO-L-LACTIDE) SURGICAL SUTURESGAMSubstantially EquivalentInternacional Farmaceutica, S.A. DE C.V.accessdata.fda.gov
June 4, 2004K041048POLYDIOXANONE SYNTHETIC ABSORBABLE SURGICAL SUTURENEWSubstantially EquivalentInternacional Farmaceutica, S.A. DE C.V.accessdata.fda.gov
April 29, 2004K040282ATRAMAT AND SORB-FAST POLYGLYCOLIC ACIDGAMSubstantially EquivalentInternacional Farmaceutica, S.A. DE C.V.accessdata.fda.gov
December 4, 1991K913185STERILE STAINLESS STEEL MONOFIL NONABSORB SURG SUTGAQSubstantially EquivalentInternacional Farmaceutica, S.A. DE C.V.accessdata.fda.gov
October 25, 1991K911354STERILE PLAIN GUT/CHROMIC GUT ABSORB SURG SUTURESGALSubstantially EquivalentInternacional Farmaceutica, S.A. DE C.V.accessdata.fda.gov
April 25, 1991K911189STERILE POLYPROPYLENE MONFIL NONABSORB SURG SUTUREGAWSubstantially EquivalentInternacional Farmaceutica, S.A. DE C.V.accessdata.fda.gov
February 11, 1991K905287IFSA STERILE SILK BRAIDED NONABSOR SURG SUTURESGAPSubstantially EquivalentInternacional Farmaceutica, S.A. DE C.V.accessdata.fda.gov
February 11, 1991K905286IFSA STERILE NLYLON MONOFIL NONABSOR SURG SUTURESGARSubstantially EquivalentInternacional Farmaceutica, S.A. DE C.V.accessdata.fda.gov
February 11, 1991K905285IFSA STERILE BRAIDED POLY NONABSOR SURG SUTURESGASSubstantially EquivalentInternacional Farmaceutica, S.A. DE C.V.accessdata.fda.gov

Compare with other makers

Updated May 23, 2008. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.