Dte,woodpecker

11 catalogue numbers from UL24, listed by Guilin Woodpecker Medical Instrument Co., Ltd., China, under Drill, Bone, Powered. 2 manufacturers in China are registered for this product code.

Registry build 21.09.26
2manufacturers in China registered for this device type
11catalogue 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 Dte,woodpecker
Listed by Guilin Woodpecker Medical Instrument Co., Ltd., China
FDA product code DZI
Device type Drill, Bone, Powered
Device class Class 2
Regulation 21 CFR 872.4120
Establishment Manufacturer
510(k) K111290
Record published 2022-08-17

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries manufacturing date

Catalogue Numbers

Catalogue numbers for Dte,woodpecker
Catalogue number Size Status
UL24 In distribution
UE5 In distribution
UL25 In distribution
UE6 In distribution
UE7 In distribution
UC8 In distribution
UE8L In distribution
UE8R In distribution
UL23 In distribution
UL17 In distribution
UL22 In distribution

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
K111290 2011-11-18

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