Symmetry Logan

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name: Symmetry Logan FDA UDI
Generic Name: Palate prosthesis FDA UDI
Device Name: Symmetry® Bow, Logan Traction, w/o Teeth, 35 mm FDA UDI
Model / Reference: 72-0920 FDA UDI
Description: Symmetry® Bow, Logan Traction, w/o Teeth, 35 mm FDA UDI

Identifiers

Catalog Number: 72-0920 FDA UDI
Primary DI / UDI-DI: 00887482122723 FDA UDI
FDA Product Code: HST FDA UDI
GMDN Term: Palate prosthesis FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.5850 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 35 Millimeter FDA UDI

Category: Palate prosthesis

Symmetry Logan by Symmetry Surgical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Palate prosthesis.

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Custom Healthcare Systems Inc. — Manus Medical, LLC · Class II
CUSTOM HEALTHCARE SYSTEMS, INC — Manus Medical, LLC · Class II
Symmetry Logan — SYMMETRY SURGICAL INC. · Class I

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 I	Pending data

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Manufacturer

Manufacturer: Symmetry Surgical Inc.

Sources (1)

FDA UDI b065eef9-bc31-4ff0-9b3a-51599b6f119e 36 fields · synced May 30, 2026