Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9680235

FEI Number

3002807188

Entity Name

ARTA PLAST AB

City/State/Country

Tyresoe Stockholm, SE

Establishment Address

Antennvaegen 1, Tyresoe Stockholm 13548, SE

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Arta Plast AB (Owner Number: 10051331)

Owner / Operator Contact Address

Antennvaegen 1, Tyresoe, SE-AB 13548, SE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DRAIN, TEE (WATER TRAP) Patellar Adjustment Socket Femoral Drilling Socket Femoral Adjustment Socket

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BYH	Drain, Tee (Water Trap)	Anesthesiology	Class 1	868.5995	2017-07-13
KRR	Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer	Orthopedic	Class 2	888.3540	2023-03-31

Official Correspondent

No official correspondent registered.

US Agent Details

Steven Crees Business: Seerc consulting Email: Steven.crees@artaplast.se Phone: (763) 6399651

Related Public Records

Same Entity

Arta Plast AB

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9680235. Last updated year: 2026. Please use registration number 9680235 when referencing this establishment in official correspondence.