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Vertical Lengthening Chin

FDA UDI

Class II (US FDA UDI)

by Implantech Associates, Inc.

Identity

Trade Name
Vertical Lengthening Chin FDA UDI
Generic Name
Chin prosthesis FDA UDI
Device Name
Chin Implant FDA UDI
Model / Reference
Size: Medium FDA UDI
Description
Chin Implant FDA UDI

Identifiers

Catalog Number
VLC-M-NS FDA UDI
Primary DI / UDI-DI
M724VLCMNS1 FDA UDI
510(k) Number
K904657 FDA UDI
K911516 FDA UDI
FDA Product Code
FWP FDA UDI
GMDN Term
Chin prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.3550 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: Chin prosthesis

Vertical Lengthening Chin by Implantech Associates, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Chin prosthesis.

Cleared under the same submission

K904657 also covers:

K911516 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Implantech Associates, Inc.

Sources (1)

  • FDA UDI ea9d5d4c-9c96-4d10-8f23-cd9810e696a1 36 fields · synced Jun 9, 2026