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Imtec

FDA UDI

Class II (US FDA UDI)

by Park Dental Research Corp

Identity

Trade Name
IMTEC FDA UDI
Generic Name
Screwing power tool attachment FDA UDI
Device Name
Lew O-Ball Latch Driver FDA UDI
Model / Reference
165DL FDA UDI
Description
Lew O-Ball Latch Driver FDA UDI

Identifiers

Catalog Number
165DL FDA UDI
Primary DI / UDI-DI
D769165DL0 FDA UDI
510(k) Number
K121707 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Screwing power tool attachment FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3640 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Screwing power tool attachment

Imtec by Park Dental Research Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Screwing power tool attachment.

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 823d5781-4fa8-4100-b59d-a3cc8999f19f 36 fields · synced Jun 1, 2026