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Symmetry Laforce

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Laforce FDA UDI
Generic Name
Adenotome FDA UDI
Device Name
Symmetry® Adenotome; Laforce; #2 Medium FDA UDI
Model / Reference
71-1012 FDA UDI
Description
Symmetry® Adenotome; Laforce; #2 Medium FDA UDI

Identifiers

Catalog Number
71-1012 FDA UDI
Primary DI / UDI-DI
00887482122242 FDA UDI
FDA Product Code
KBH FDA UDI
GMDN Term
Adenotome FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Adenotome

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

Similar devices

Also classified as Adenotome.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Symmetry Surgical Inc.

Sources (1)

  • FDA UDI cbd7a6be-ca77-4042-9efc-853a8752ea75 35 fields · synced May 30, 2026