MECTRON
- Primary DI
- E32202900137
- Brand
- MECTRON
- Company
- MECTRON SPA
- Model
- K10
- Catalog number
- 02900137-001
- Device description
- K10 is a torque wrench used for tightening inserts to the Mectron ultrasonic handpieces.
- Published
- 2019-09-10
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| ELC | Scaler, Ultrasonic |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| ELC | Scaler, Ultrasonic | Dental | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K140965 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| E32202900137 | Direct Marking | HIBCC | 0 | |
| E322029001370010 | Primary | HIBCC | 0 |
GMDN Terms#
| Term | Definition |
|---|---|
| Ultrasonic surgical system torque wrench, reusable | A hand-held instrument designed to manually attach or detach a handpiece tip (blade) from the handpiece of an ultrasonic surgical system. It is typically formed with a socket that is placed over the handpiece tip and rotated by the operator to tighten or loosen, with appropriate torque, the tip to or from the handpiece. The device is made of durable materials and typically includes a mechanism to prevent under- or over-tightening. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1 6144594922 | info@piezosurgery.us |
Regulatory Flags#
- DUNS number
- 436664734
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- false
- Serial number
- false
- Manufacturing date on label
- true
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| E322036000220 | MECTRON | MT1817L | 03600022 | 2026-04-20 |
| E322036300090 | MECTRON | MF1004L | 03630009 | 2026-04-20 |
| E322033800150 | MECTRON | OP1125 | 03380015 | 2026-02-18 |
| E322033800160 | MECTRON | OP1225 | 03380016 | 2026-02-18 |
| E322034000110 | MECTRON | EX0410 | 03400011 | 2026-02-18 |
| E322034000120 | MECTRON | EX0510 | 03400012 | 2026-02-18 |
| E322034000130 | MECTRON | EX0610 | 03400013 | 2026-02-18 |
| E322048000111010 | MECTRON | PD0620A -US- | 04800011-101 | 2026-02-18 |
| E322048000121010 | MECTRON | PD0620B -US- | 04800012-101 | 2026-02-18 |
| E322051000851010 | MECTRON | starlight pro - SHINY YELLOW -USA | 05100085-101 | 2025-06-17 |
| E322051000861010 | MECTRON | starlight pro - MATT BLACK -USA | 05100086-101 | 2025-06-17 |
| E322051000871010 | MECTRON | starlight pro - SHINY SILVER -USA | 05100087-101 | 2025-06-17 |
| E322031202490010 | MECTRON | MANIPOLO PIEZOSURGERY® medical + | 03120249-001 | 2025-06-16 |
| E322036300080 | MECTRON | MF0804+ | 03630008 | 2025-06-16 |
| E322051000831010 | MECTRON | starlight pro - SHINY WHITE -USA | 05100083-101 | 2025-06-16 |
| E322048000011010 | MECTRON | PD0118A -US- | 04800001-101 | 2024-10-15 |
| E322048000021010 | MECTRON | PD0223A -US- | 04800002-101 | 2024-10-15 |
| E322048000031010 | MECTRON | PD0328A -US- | 04800003-101 | 2024-10-15 |
| E322048000041010 | MECTRON | PD0432A -US- | 04800004-101 | 2024-10-15 |
| E322048000051010 | MECTRON | PD0535A -US- | 04800005-101 | 2024-10-15 |
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