← Back to catalogue

ContourFlex™ Gluteal Implant, Round

FDA UDI

Class II (US FDA UDI)

by Implantech Associates, Inc.

Identity

Trade Name
ContourFlex™ Gluteal Implant, Round FDA UDI
Generic Name
Silicone-block tissue reconstructive material FDA UDI
Device Name
Contoured Carving Block Implant FDA UDI
Model / Reference
size6 FDA UDI
Description
Contoured Carving Block Implant FDA UDI

Identifiers

Catalog Number
CCB5-6 FDA UDI
Primary DI / UDI-DI
M724CCB561 FDA UDI
510(k) Number
K052504 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

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Silicone-block tissue reconstructive material

ContourFlex™ Gluteal Implant, Round 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI bddcdc4a-a573-4778-bcba-7509e4a8a3c5 36 fields · synced Jun 9, 2026