Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013546453

FEI Number

3013546453

Entity Name

AVANTTI MEDI CLEAR MBP, S.A.P.I. DE C.V.

City/State/Country

Tijuana Baja California, MX

Establishment Address

CAMINO VECINAL 2461, MURUA ORIENTE, Tijuana Baja California 22465, MX

Establishment Type(s)

Sterilize Medical Device for Another Party (Contract Sterilizer)

Owner / Operator

AVANTTI MEDI CLEAR MBP, S.A.P.I. DE C.V. (Owner Number: 10053515)

Owner / Operator Contact Address

CAMINO VECINAL 2461, MURUA ORIENTE, Tijuana, MX-BCN 22465, MX

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

LABOMEX MBP Catheter Catheter

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JRC	Micro Pipette	Clinical Chemistry	Class 1	862.2050	2017-12-18
FMK	Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature	General, Plastic Surgery	Class 2	878.4850	2026-04-08
LOX	Catheters, Transluminal Coronary Angioplasty, Percutaneous	Cardiovascular	Class 2	870.5100	2020-09-25
LOX	Catheters, Transluminal Coronary Angioplasty, Percutaneous	Cardiovascular	Class 2	870.5100	2020-09-25
GAZ	Tubing, Noninvasive	General Hospital	Class 2	880.6740	2021-06-08

Official Correspondent

Enrique Garcia

US Agent Details

FERNANDO LUNA Email: fluna@avanttimediclear.com Phone: (619) 9728639

Related Public Records

Same Entity

AVANTTI MEDI CLEAR MBP, S.A.P.I. DE C.V.

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3043534762	AVANTTI MEDI CLEAR MBP, S.A.P.I. DE C.V.	TIJUANA Baja California, MX

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K130132	Medipurpose Pte. , Ltd.	BABYLANCE HEEL INCISION DEVICE	2013-02-11
K910471	Baxter Healthcare Corp	MEDID-VAC CLEAR NONCONDUCTIVE CONNECTING TUBE	1991-03-08

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0044-2008	Becton Dickinson & Company	2	Microtainer Safety Flow Lancets; Green Sterile, Use Once and Discard; 1.4 mm Blade Length; 1.0mm Blade Width; Becton Dickinson Vacutainer Systems; Becton Dickinson & Company; Franklin Lakes, NJ 07417
Z-0030-04	N/A	2	Ace Percutaneous Transluminal Coronary Angioplasty (PTCA) Dilatation Catheter with 2cm Tip 20 mm Balloon, Catalog Number H74902071011
Z-0031-04	N/A	2	Ace Percutaneous Transluminal Coronary Angioplasty (PTCA) Dilatation Catheter with 2cm Tip 20 mm Balloon, Catalog Number H74902071051
Z-0032-04	N/A	2	Ace Percutaneous Transluminal Coronary Angioplasty (PTCA) Dilatation Catheter with 1 cm Tip and 20 mm Balloon, Catalog Number H74903628151

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013546453. Last updated year: 2026. Please use registration number 3013546453 when referencing this establishment in official correspondence.