MD 30

Dental implant motor system, SET

Registry build 21.09.26
2manufacturers in China registered for this device type
17catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Guangxi (1), Guangdong (1).

Chinese manufacturers registered for FDA product code DZI
Manufacturer City Province Registered as Device types
Guilin Woodpecker Medical Instrument Co., Ltd. Guilin Guangxi Manufacturer 25
Guangdong Jinme Medical Technology Co., Ltd. Foshan Guangdong Manufacturer 13

Record

Regulatory record for MD 30
Listed by Nouvag AG, Switzerland
FDA product code DZI
Device type Drill, Bone, Powered
Device class Class 2
Regulation 21 CFR 872.4120
Establishment Private-label distributor, Manufacturer, Exporter
510(k) K042434
Record published 2017-01-13
Record revised 2018-08-20 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries manufacturing date, serial number
Distribution end date 2017-12-04

Catalogue Numbers

Catalogue numbers for MD 30
Catalogue number Size Status
3330SAL In distribution
2005 In distribution
2016IMP In distribution
3330IDI In distribution
2016 In distribution
2005IDI In distribution
2007SAL In distribution
2004SAL In distribution
2016IDI In distribution
3330 In distribution
2007 In distribution
2004 In distribution
2004IDI In distribution
3330IMP In distribution
2005CAM Withdrawn
3330CAM Withdrawn
2004CAM Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Drill, Bone, Powered Synthes Gmbh 150
Acteon Satelec 87
Neoss Implant System Neoss AB 74
Mectron Mectron SPA 48
OneDrill Surgical Drill Osseofuse International Inc. 48
Silfradent srl Silfradent SRL 45
MatrixMANDIBLE Synthes Gmbh 31
DIRECTguide™ Step Drill Implant Direct Sybron Manufacturing LLC 31
DIRECTguide™ Guided Step Drill Implant Direct Sybron Manufacturing LLC 30
Woodpecker Guilin Woodpecker Medical Instrument Co., Ltd. 28
VarioSurg Nakanishi Inc. 22
Nobel Biocare® Nobel Biocare AB 20

Showing 12 of 265. All products under Drill, Bone, Powered

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K042434 2004-11-03

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