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Surgical Instrument

FDA UDI

Class II (US FDA UDI)

by S.I.N. - Sistema DE Implante Nacional S.A.

Identity

Trade Name
SURGICAL INSTRUMENT FDA UDI
Generic Name
Dental torque wrench FDA UDI
Device Name
SURGICAL TORQUE FIXER FDA UDI
Model / Reference
TMECC FDA UDI
Description
SURGICAL TORQUE FIXER FDA UDI

Identifiers

Catalog Number
TMECC FDA UDI
Primary DI / UDI-DI
07899995215116 FDA UDI
510(k) Number
K201688 FDA UDI
FDA Product Code
KCT FDA UDI
GMDN Term
Dental torque wrench FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental torque wrench

Surgical Instrument by S.I.N. - Sistema DE Implante Nacional S.A. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental torque wrench.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ef6b87c7-3216-46fb-89c3-bb7f70e5f3b6 35 fields · synced May 30, 2026