PRIMUS Sterilizer Company LLC

FDA Device Registration & Listing · Sanford, FL, US · Registration 3030597797

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
3030597797
FEI Number
3030597797
Entity Name
PRIMUS Sterilizer Company LLC
City/State/Country
Sanford, FL, US
Establishment Address
110 Tech Dr, Sanford, FL 32771, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Primus (Owner Number: 9005293)
Owner / Operator Contact Address
110 Tech Dr, Sanford, FL 32771, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K093333
PMA Number
N/A

All Registered Proprietary Names

Primus Sterilizer PSS11-HA Primus Sterilizer PSS11-HB Sterilizer,steam two one

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FLE Sterilizer, Steam General Hospital Class 2 880.6880 2023-12-20
FLE Sterilizer, Steam General Hospital Class 2 880.6880 2023-11-03
FLE Sterilizer, Steam General Hospital Class 2 880.6880 2019-02-25
FLE Sterilizer, Steam General Hospital Class 2 880.6880 2019-02-25

Official Correspondent

Subramanian Hariharan

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
1932355 PRIMUS STERILIZER COMPANY, LLC. Great Bend, KS, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K021223 Sauter AG BELIMED STEAM STERILIZER, MODEL TOP 5000 2002-06-26
K050263 M.O. Com S.R.L. MILLENNIUM SERIES, INCLUDING MILLENNIUM B, B+, B2 AND BU 2006-11-21

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030597797. Last updated year: 2026. Please use registration number 3030597797 when referencing this establishment in official correspondence.
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