SAINT-GOBAIN PERFORMANCE PLASTICS CORPORATION

FDA Device Registration & Listing · Largo, FL, US · Registration 3021186084

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
3021186084
FEI Number
3021186084
Entity Name
SAINT-GOBAIN PERFORMANCE PLASTICS CORPORATION
City/State/Country
Largo, FL, US
Establishment Address
8615 126th Avenue North, Ste 650, Largo, FL 33773, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Saint-Gobain Performance Plastics Corporation (Owner Number: 10083372)
Owner / Operator Contact Address
8615 126th Avenue North, Ste 650, Largo, FL 33773, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KJE Spinner System, Cell Culture Hematology Class 1 864.2240 2021-11-15
KJC Bottle, Roller, Tissue Culture Hematology Class 1 864.2240 2021-11-15
KJA Flask, Tissue Culture Hematology Class 1 864.2240 2021-11-15

Official Correspondent

Ileana Irizarry

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Saint-Gobain Performance Plastics Corporation
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Similar Registrations

Registration Number Establishment Name Location
3008624479 MEDIKAN CO., Ltd. Gangseo-gu Seoul, KR
3011777678 CORNING INCORPORATED Tewksbury, MA, US
1319660 ISOMEDIX OPERATIONS INC. CHESTER, NY, US
1218905 CORNING-KENNEBUNK KENNEBUNK, ME, US
1423662 Sterigenics US LLC Gurnee, IL, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021186084. Last updated year: 2026. Please use registration number 3021186084 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.