SIENTRA Dual Magnetic Port Locator

FDA UDI

Class U (US FDA UDI)

by Sientra, Inc.

Identity

Trade Name: SIENTRA Dual Magnetic Port Locator FDA UDI
Generic Name: Skin-port tissue expander FDA UDI
Device Name: Dual Magnetic Port Locator FDA UDI
Model / Reference: DMPL01 FDA UDI
Description: Dual Magnetic Port Locator FDA UDI

Identifiers

Catalog Number: DMPL01 FDA UDI
Primary DI / UDI-DI: 00819409021987 FDA UDI
FDA Product Code: LCJ FDA UDI
GMDN Term: Skin-port tissue expander FDA UDI

Classification

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

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Skin-port tissue expander Tissue expander injection port locator

SIENTRA Dual Magnetic Port Locator by Sientra, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tissue expander injection port locator.

TRUSITE® — Pmt Corp. · Class I
MENTOR CENTERSCOPE Magnetic Detection Device — Mentor Texas LP · U
Precision Point Locator — Sientra, Inc. · U
AlloX2 Magnetic Site Locator — Sientra, Inc. · U
Tissue Expander Remote Port Accessories — Sientra, Inc. · U

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class U	Pending data

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

Manufacturer

Manufacturer: Sientra, Inc.

Sources (1)

FDA UDI 22c384e4-8853-4e52-ba5a-62e55297f64a 36 fields · synced May 30, 2026