GENZYME CORPORATION

FDA Device Registration & Listing · Ridgefield, NJ, US · Registration 3039908023

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
3039908023
FEI Number
3039908023
Entity Name
GENZYME CORPORATION
City/State/Country
Ridgefield, NJ, US
Establishment Address
1125 PLEASANTVIEW TERRACE, Ridgefield, NJ 07657, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
GENZYME CORPORATION (Owner Number: 9002116)
Owner / Operator Contact Address
450 Water Street, Cambridge, MA 02141, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
P940015

All Registered Proprietary Names

Synvisc/SynviscOne

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MOZ Acid, Hyaluronic, Intraarticular Unknown Class 3 N/A 2003-06-30

Official Correspondent

Kathleen Holdren

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
1220423 GENZYME CORPORATION FRAMINGHAM, MA, US
3009389940 GENZYME COPORATION Northborough, MA, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3039908023. Last updated year: 2026. Please use registration number 3039908023 when referencing this establishment in official correspondence.
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