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OPUS Silicone Gel Breast Implant Sizer

FDA UDI

Class U (US FDA UDI)

by Sientra, Inc.

Identity

Trade Name
OPUS Silicone Gel Breast Implant Sizer FDA UDI
Generic Name
Invasive breast implant sizer, fixed, single-use FDA UDI
Device Name
Silicone Gel Breast Implant Sizer, Smooth Round, Moderate Plus Projection, 385 cc FDA UDI
Model / Reference
GS10621-385MP FDA UDI
Description
Silicone Gel Breast Implant Sizer, Smooth Round, Moderate Plus Projection, 385 cc FDA UDI

Identifiers

Catalog Number
GS10621-385MP FDA UDI
Primary DI / UDI-DI
00819409023905 FDA UDI
510(k) Number
K200706 FDA UDI
FDA Product Code
MRD FDA UDI
GMDN Term
Invasive breast implant sizer, fixed, single-use FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Invasive breast implant sizer, fixed, single-use

OPUS Silicone Gel Breast Implant Sizer by Sientra, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Invasive breast implant sizer, fixed, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sientra, Inc.

Sources (1)

  • FDA UDI 3a2e8eff-239f-4559-9ab8-5240e2c9b8c0 37 fields · synced May 30, 2026