Cement Restrictor

2 catalogue numbers from EBO100, listed by Tornier Inc., United States, under Cement Obturator. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
2catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Shanghai (2), Jiangsu (1).

Chinese manufacturers registered for FDA product code LZN
Manufacturer City Province Registered as Device types
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34

Record

Regulatory record for Cement Restrictor
Listed by Tornier Inc., United States
FDA product code LZN
Device type Cement Obturator
Device class Class 2
Regulation 21 CFR 878.3300
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer, Exporter
Record published 2015-10-16
Record revised 2024-10-29 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries expiry date, manufacturing date, serial number
Sizes Outer diameter 13 to 38 mm

Catalogue Numbers

Catalogue numbers for Cement Restrictor
Catalogue number Size Status
EBO100 Outer Diameter 38 mm In distribution
EBO102 Outer Diameter 13 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Clearcut Teknimed SAS 13
Exeter Howmedica Osteonics Corp 11
Cement Obturator Zimmer, Inc. 10
Buck Smith & Nephew, Inc. 8
DJO Surgical Encore Medical, L.P. 6
Spectron Smith & Nephew, Inc. 6
Cemstop Teknimed SAS 6
MectaPlug Teknimed SAS 6
Biostop Depuy Orthopaedics, Inc. 5
Bone Plug Howmedica Osteonics Corp 3
ACM BioPrep Stryker GmbH 2
Perfecta Microport Orthopedics Inc. 2

Showing 12 of 17. All products under Cement Obturator

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K061824 2006-09-14

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer