MESCO, INC.

FDA Device Registration & Listing · Pasig City National Capital Region, PH · Registration 3009662565

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3009662565
FEI Number
3009662565
Entity Name
MESCO, INC.
City/State/Country
Pasig City National Capital Region, PH
Establishment Address
Reliance cor. Brixton Sts., Kapitoyo, Pasig City National Capital Region 1603, PH
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
MESCO, INC. (Owner Number: 10057990)
Owner / Operator Contact Address
Reliance cor. Brixton Sts., Kapitoyo, Pasig City, PH-00 1603, PH
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Bone Plates

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HRS Plate, Fixation, Bone Orthopedic Class 2 888.3030 2023-10-27

Official Correspondent

David Lee

US Agent Details

Anna Savillo Email: asavillo@icloud.com Phone: (856) 2786325

Related Public Records

Same Entity

MESCO, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K042598 Zimmer, Inc. PERIARTICULAR LOCKING PLATES AND SCREWS, 2357 AND 2359 SERIES 2004-10-29
K190842 Jiangsu Trauhui Medical Instrument Co., Ltd. Comus Locking Plate systems 2020-02-03
K130510 Arthrex, Inc. ARTHREX COMPRESSION PLATES 2013-09-25
K202803 Newclip Technics Activmotion S DTO 2021-12-16

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0034-2022 Flower Orthopedics Corporation 2
Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009662565. Last updated year: 2026. Please use registration number 3009662565 when referencing this establishment in official correspondence.
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