SAFETEC OF AMERICA, INC.

FDA Device Registration & Listing · BUFFALO, NY, US · Registration 1319744

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
1319744
FEI Number
1000159898
Entity Name
SAFETEC OF AMERICA, INC.
City/State/Country
BUFFALO, NY, US
Establishment Address
887 Kensington Avenue, BUFFALO, NY 14215, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Safetec of America Inc (Owner Number: 9006898)
Owner / Operator Contact Address
887 KENSINGTON AVENUE, --, Buffalo, NY 14215, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Protective Barrier Wipes Adhesive Remover Wipes

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KOX Solvent, Adhesive Tape General, Plastic Surgery Class 1 878.4730 2018-10-15

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Safetec of America 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
2417346 TORBOT, A Division of Safetec CRANSTON, RI, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1319744. Last updated year: 2026. Please use registration number 1319744 when referencing this establishment in official correspondence.
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