Symmetry Surgical

FDA UDI

Class II (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name: Symmetry Surgical FDA UDI
Generic Name: Laparoscopic surgery handle FDA UDI
Device Name: Handle, 5.0 mm Thumb Ring Handle, Kleppinger Type, 31.7 cm FDA UDI
Model / Reference: 90-1013 FDA UDI
Description: Handle, 5.0 mm Thumb Ring Handle, Kleppinger Type, 31.7 cm FDA UDI

Identifiers

Primary DI / UDI-DI: 00887482128596 FDA UDI
510(k) Number: K113080 FDA UDI
FDA Product Code: HIN FDA UDI
GMDN Term: Laparoscopic surgery handle FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 884.4150 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

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 — 31.7 Centimeter FDA UDI

Category: Laparoscopic surgery handle

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

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Also classified as Laparoscopic surgery handle.

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ELMED — ELMED INCORPORATED · Class II
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Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
ELMED — ELMED INCORPORATED · Class II

Cleared under the same submission

K113080 also covers:

Symmetry Surgical — SYMMETRY SURGICAL INC.

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 II	Pending data

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Manufacturer

Manufacturer: Symmetry Surgical Inc.

Sources (1)

FDA UDI 8d32c644-358c-4177-8b50-87cce2b5077f 36 fields · synced May 30, 2026