EXSURCO MEDICAL, INC.

FDA Device Registration & Listing · Wakeman, OH, US · Registration 3011981870

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
3011981870
FEI Number
3011981870
Entity Name
EXSURCO MEDICAL, INC.
City/State/Country
Wakeman, OH, US
Establishment Address
10804 GREEN RD, Wakeman, OH 44889, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Exsurco Medical, Inc. (Owner Number: 10053475)
Owner / Operator Contact Address
10804 Green Road, Wakeman, OH 44889, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Amalgatome® SD mesh ex® carrier mesh ex® MeshEx Skin Graft Carrier

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GFD Dermatome General, Plastic Surgery Class 1 878.4820 2016-12-08
FZW Expander, Surgical, Skin Graft General, Plastic Surgery Class 1 878.4800 2023-04-24
GEJ Carrier, Ligature General, Plastic Surgery Class 1 878.4800 2025-12-09

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Exsurco Medical, Inc.
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 3011981870. Last updated year: 2026. Please use registration number 3011981870 when referencing this establishment in official correspondence.
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