K. W. GRIFFEN CO.

FDA Device Registration & Listing · NORWALK, CT, US · Registration 1211177

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
1211177
FEI Number
1211177
Entity Name
K. W. GRIFFEN CO.
City/State/Country
NORWALK, CT, US
Establishment Address
100 PEARL ST., NORWALK, CT 06850, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
K. W. GRIFFEN CO. (Owner Number: 1211177)
Owner / Operator Contact Address
100 PEARL ST., --, Norwalk, CT 06850, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MetriSponge Brush

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FRL Fiber, Medical, Absorbent General Hospital Class 1 880.5300 1992-08-27
GEC Brush, Scrub, Operating-Room General, Plastic Surgery Class 1 878.4800 1992-08-27

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

K. W. GRIFFEN CO.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1211177. Last updated year: 2026. Please use registration number 1211177 when referencing this establishment in official correspondence.
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