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SIENTRA Chin Implant

FDA UDI

Class II (US FDA UDI)

by Sientra, Inc.

Identity

Trade Name
SIENTRA Chin Implant FDA UDI
Generic Name
Chin prosthesis FDA UDI
Device Name
Chin Implant, Solid Silicone, Smooth, 53 mm FDA UDI
Model / Reference
10-055U FDA UDI
Description
Chin Implant, Solid Silicone, Smooth, 53 mm FDA UDI

Identifiers

Catalog Number
10-055U FDA UDI
Primary DI / UDI-DI
00812790023271 FDA UDI
510(k) Number
K981850 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
Not 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Length — 53 Millimeter FDA UDI

SIENTRA Chin Implant by Sientra, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sientra, Inc.

Sources (1)

  • FDA UDI f707812d-0e9a-4518-b91b-c652cbc24826 38 fields · synced Jun 8, 2026