POLY-MED, INC.

FDA Device Registration & Listing · Piedmont, SC, US · Registration 3020659113

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
3020659113
FEI Number
3020659113
Entity Name
POLY-MED, INC.
City/State/Country
Piedmont, SC, US
Establishment Address
116 Leader Drive, Piedmont, SC 29673, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Poly-Med, Inc. (Owner Number: 10034488)
Owner / Operator Contact Address
51 Technology Drive, Anderson, SC 29625, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Restrata Cerafix Dura Substitute

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QSZ Absorbable Synthetic Wound Dressing Unknown Class U N/A 2018-11-29
GXQ Dura Substitute Neurology Class 2 882.5910 2020-03-12

Official Correspondent

Eric Cochran

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Poly-Med, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3006121828 POLY-MED, INC. Anderson, SC, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020659113. Last updated year: 2026. Please use registration number 3020659113 when referencing this establishment in official correspondence.
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