Atlas FDA

ULTRASONIC SURGERY MACHINE

FDA 510(k) clearance K113152 · decided 2012-06-14

Clearance details

K-number
K113152
Device name
ULTRASONIC SURGERY MACHINE
Applicant
Dmetec.Co., Ltd.
Decision
Substantially Equivalent
Date received
2011-10-25
Decision date
2012-06-14
Days to decision
233 days
Clearance type
Traditional
Product code
DZI
Device class
2
Regulation number
872.4120
Medical specialty
Dental
Advisory committee
Dental
Location
Glendale, CA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Angled Screwdriver MED (M-SD090) (K253655)W&H Dentalwerk Bürmoos GmbH2026-07-31
Implantmed Plus II & Piezomed Plus II Module (K253776)W&H Dentalwerk Buermoos GmbH2026-06-18
VarioSurg 4 (K254163)Nakanishi, Inc.2025-12-23
MT-Bone (K242432)Mectron S.P.A.2024-08-19
Surgical Drive System (Model: ES70, ES90, E8) (K240340)Guangdong Jinme Medical Technology Co., Ltd.2024-07-18
Guided Surgery Kit (K231087)Implant Direct Sybron Manufacturing, LLC2023-08-16
TRAUS SUS20 (K192561)Saeshin Precision Co., Ltd.2020-07-13
Surgical Drills (K200265)Implant Direct Sybron Manufacturing, LLC2020-06-30
Contour P-Insert 90, Contour P-Insert 45, Contour P-Insert Tri Tip, Contour P-Insert WC Tip, Contour P-Insert Quad Tip (K192033)Bennett Jacoby, Dds, Ms, Inc.2020-06-09
PIEZOTOME CUBE (K172137)Satelec - Acteon Group2018-05-03
Piezosurgery White (K171326)Mectron S.P.A.2018-04-13
PIEZOSURGERY TOUCH, PIEZOSURGERY WHITE (K171958)Mectron S.P.A.2018-01-12

Recalls involving this device

No recalls on record reference this clearance.