CURRIER MOS PLASTICS LLC

FDA Device Registration & Listing · San Jose, CA, US · Registration 3008513917

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
3008513917
FEI Number
3008513917
Entity Name
CURRIER MOS PLASTICS LLC
City/State/Country
San Jose, CA, US
Establishment Address
2308 Zanker Rd, San Jose, CA 95131, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Currier MOS Plastics LLC (Owner Number: 10093230)
Owner / Operator Contact Address
2308 Zanker Road, San Jose, CA 95131, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SportPort 8.5 x 6 SportPort 6.5 x 6 ClearVu 2.7 Sharp TwoVu ST-6 TwoVu ST-5 ClearVu 2.7 Blunt EntreVu EX-8-7T TwoVu ST-6L ExtravaStopper Talarus

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NBH Accessories, Arthroscopic Orthopedic Class 1 888.1100 2026-03-04
FGY Cannula, Injection General, Plastic Surgery Class 1 878.4200 2026-03-04
GEA Cannula, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2026-03-04

Official Correspondent

Michael Rashidian

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Currier MOS Plastics LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K863293 Lifestream Int'L, Inc. DISPOSABLE SUCTION CANNULA NO. 902008-000 1986-09-09

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0040-2011 Smith & Nephew, Inc. Endoscopy Division 1
Smith & Nephew Aimer Endofemoral 3mm Offset (Blue) Catalog Number: 72201713 ACUFEX Surgical Instruments are intended for use in orthopedic and general surgery.
Z-0041-2011 Smith & Nephew, Inc. Endoscopy Division 1
Smith & Nephew Aimer Endofemoral 4mm Offset (Purple Catalog Number: 72201714 ACUFEX Surgical Instruments are intended for use in orthopedic and general surgery.
Z-0042-2011 Smith & Nephew, Inc. Endoscopy Division 1
Smith & Nephew Aimer Endofemoral 5mm Offset (Red) Catalog Number: 72201715 ACUFEX Surgical Instruments are intended for use in orthopedic and general surgery.
Z-0043-2011 Smith & Nephew, Inc. Endoscopy Division 1
Smith & Nephew Aimer Endofemoral 6mm Offset (Green) Catalog Number: 72201716 ACUFEX Surgical Instruments are intended for use in orthopedic and general surgery.
Z-0044-2011 Smith & Nephew, Inc. Endoscopy Division 1
Smith & Nephew Aimer Endofemoral 7mm Offset (Gold) Catalog Number: 72201717 ACUFEX Surgical Instruments are intended for use in orthopedic and general surgery.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008513917. Last updated year: 2026. Please use registration number 3008513917 when referencing this establishment in official correspondence.
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