← Back to catalogue

Symmetry Sinskey

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Sinskey FDA UDI
Generic Name
Soft-tissue surgical hook, reusable FDA UDI
Device Name
Symmetry® Hook, Sinskey Lens Manipulating FDA UDI
Model / Reference
60-9513T FDA UDI
Description
Symmetry® Hook, Sinskey Lens Manipulating FDA UDI

Identifiers

Catalog Number
60-9513T FDA UDI
Primary DI / UDI-DI
00887482112571 FDA UDI
FDA Product Code
HNQ FDA UDI
GMDN Term
Soft-tissue surgical hook, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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: Soft-tissue surgical hook, reusable

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

Similar devices

Also classified as Soft-tissue surgical hook, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Sources (1)

  • FDA UDI 729b3c9c-285e-4638-b170-bce45d942eb3 35 fields · synced May 30, 2026