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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
Surgical instrument/implant rack FDA UDI
Device Name
Lew MDI Case FDA UDI
Model / Reference
IM-CASE-4 FDA UDI
Description
Lew MDI Case FDA UDI

Identifiers

Catalog Number
CASE-4 FDA UDI
Primary DI / UDI-DI
D769IMCASE40 FDA UDI
510(k) Number
K121707 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Surgical instrument/implant rack 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: Surgical instrument/implant rack

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

Similar devices

Also classified as Surgical instrument/implant rack.

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 2e4e6007-6a5a-4c5c-90d3-ce1811df986c 36 fields · synced Jun 8, 2026