X-SG93

The X-SG93 is a Ti-Max Series Oral Surgery Contra handpiece. The FDA summary identifies it as a contra-angle handpiece for clinical use. The X-SG93 model is designed for ISO Type 3 FG…

Registry build 21.09.26

The X-SG93 is a Ti-Max Series Oral Surgery Contra handpiece. The FDA summary identifies it as a contra-angle handpiece for clinical use.

The X-SG93 model is designed for ISO Type 3 FG surgical burs. Its filing identifies oral surgery and preparation for dental implant operation as the setting and purpose.

Device Role and Details

The handpieces are driven by a micromotor and rotate surgical burs at different transmission ratios to cut maxillary or mandibular bone.

For the X-SG93 specifically, the source lists a 1:3 increasing transmission ratio and a maximum speed of 120,000 min-1.

1manufacturer
1catalogue number
2510(k) clearances naming this product code
8recalls on this code

Who Else Makes It

Registered in Guangdong.

Chinese manufacturers registered for FDA product code KMW
Manufacturer City Province Registered as Device types
Foshan Coxo Medical Instrument Co., Ltd. Foshan Guangdong Manufacturer 19

Record

Regulatory record for X-SG93
Listed by Nakanishi Inc., Japan
FDA product code KMW
Device type Handpiece, Rotary Bone Cutting
Device class Class 2
Regulation 21 CFR 872.4120
Establishment Contract manufacturer, Manufacturer
510(k) K211584
Record published 2022-02-17
Record revised 2023-10-20 (version 2)

Specifications

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

Catalogue Numbers

Catalogue numbers for X-SG93
Catalogue number Size Status
X-SG93 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
OsteoMed Osteomed 297
Ti-Max X Nakanishi Inc. 19
Micro Surgery Handpiece Nakanishi Inc. 4
Turning Handle W&H Dentalwerk Bürmoos GmbH 4
SGM-ER32i Nakanishi Inc. 3
Ti-Max Nakanishi Inc. 3
SM3 Osstem Implant Co., Ltd._Gasan Branch 3
SGQ-H Nakanishi Inc. 3
Sgms-I Nakanishi Inc. 2
S-Max M Nakanishi Inc. 2
SGM-I Nakanishi Inc. 2
SGM-ER16i Nakanishi Inc. 2

Showing 12 of 93. All products under Handpiece, Rotary Bone Cutting

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K211584 2021-08-19
K171155 2017-11-21

Recalls

8 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2018-06-01 Class II Device Design Reprocessing instructions for the SGS/SGA Surgical Handpieces have been updated with instructions of manual cleaning and specific parameters for autoclave sterilization. The previous operation manuals associated with the SGS/SGA products m 1662 2021-04-28
2018-06-01 Class II Device Design Reprocessing instructions for the SGS/SGA Surgical Handpieces have been updated with instructions of manual cleaning and specific parameters for autoclave sterilization. The previous operation manuals associated with the SGS/SGA products 18 2021-04-28
2018-06-01 Class II Device Design Reprocessing instructions for the SGS/SGA Surgical Handpieces have been updated with instructions of manual cleaning and specific parameters for autoclave sterilization. The previous operation manuals associated with the SGS/SGA products m 440 2021-04-28
2018-06-01 Class II Device Design Reprocessing instructions for the SGS/SGA Surgical Handpieces have been updated with instructions of manual cleaning and specific parameters for autoclave sterilization. The previous operation manuals associated with the SGS/SGA products m 6 2021-04-28
2018-06-01 Class II Device Design Reprocessing instructions for the SGS/SGA Surgical Handpieces have been updated with instructions of manual cleaning and specific parameters for autoclave sterilization. The previous operation manuals associated with the SGS/SGA products m 1878 2021-04-28
2018-06-01 Class II Device Design Reprocessing instructions for the SGS/SGA Surgical Handpieces have been updated with instructions of manual cleaning and specific parameters for autoclave sterilization. The previous operation manuals associated with the SGS/SGA products m 2419 2021-04-28
2018-06-01 Class II Device Design Reprocessing instructions for the SGS/SGA Surgical Handpieces have been updated with instructions of manual cleaning and specific parameters for autoclave sterilization. The previous operation manuals associated with the SGS/SGA products 12 2021-04-28
2018-06-01 Class II Device Design Reprocessing instructions for the SGS/SGA Surgical Handpieces have been updated with instructions of manual cleaning and specific parameters for autoclave sterilization. The previous operation manuals associated with the SGS/SGA products 0 2021-04-28

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