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Contoured Carving Block

FDA UDI

Class II (US FDA UDI)

by Implantech Associates, Inc.

Identity

Trade Name
Contoured Carving Block FDA UDI
Generic Name
Silicone-block tissue reconstructive material FDA UDI
Device Name
Contoured Carving Block, Style 2 FDA UDI
Model / Reference
CCB2 / Size 2 FDA UDI
Description
Contoured Carving Block, Style 2 FDA UDI

Identifiers

Catalog Number
CCB2-2-NS FDA UDI
Primary DI / UDI-DI
M724CCB22NS1 FDA UDI
510(k) Number
K952706 FDA UDI
FDA Product Code
MIB FDA UDI
GMDN Term
Silicone-block tissue reconstructive material FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3620 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Silicone-block tissue reconstructive material

Contoured Carving Block by Implantech Associates, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Silicone-block tissue reconstructive material.

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 5b151a4a-3093-4819-9df1-7ead8a20dcc7 36 fields · synced Jun 9, 2026