Power-Flo®

Catalogue number 5069-08, listed by Zimmer, Inc., United States, under Dispenser, Cement. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

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

Chinese manufacturers registered for FDA product code KIH
Manufacturer City Province Registered as Device types
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Jiangsu Changmei Medtech Co., Ltd. Changzhou Jiangsu Contract manufacturer 8
Guangzhou Clean Medical Products Manufacturing Corp Guangzhou Guangdong Contract manufacturer 5

Record

Regulatory record for Power-Flo®
Listed by Zimmer, Inc., United States
FDA product code KIH
Device type Dispenser, Cement
Device class Class 1
Regulation 21 CFR 888.4200
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer, Exporter
Premarket notification Exempt
Record published 2016-07-25
Record revised 2023-05-03 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Latex Contains natural rubber latex
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for Power-Flo®
Catalogue number Size Status
5069-08 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Dispenser, Cement Medtronic Sofamor Danek, Inc. 14
Pressurizer Adler Ortho SpA 11
DJO Surgical Encore Medical, L.P. 7
Vortex Smith & Nephew, Inc. 6
Dispenser, Cement Zimmer, Inc. 5
Miller™ Zimmer, Inc. 5
Dispenser, Cement Synthes (U.S.A.) LP 5
SpineJack Stryker GmbH 4
Kyphon® Cement Delivery System Medtronic Sofamor Danek, Inc. 4
Medtronic Reusable Instruments Medtronic Sofamor Danek, Inc. 4
PowerFlo Zimmer, Inc. 4
Palamix® Heraeus Medical LLC 3

Showing 12 of 111. All products under Dispenser, Cement

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K780266 1978-02-28

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