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Symmetry QUAD-LOCK®

FDA UDI

Class II (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry QUAD-LOCK® FDA UDI
Generic Name
Sterilization container filter, single-use FDA UDI
Device Name
Quadlock Filters; Polyproylene; Single Use; (1000/bx) FDA UDI
Model / Reference
50-9011 FDA UDI
Description
Quadlock Filters; Polyproylene; Single Use; (1000/bx) FDA UDI

Identifiers

Catalog Number
50-9011 FDA UDI
Primary DI / UDI-DI
00887482141403 FDA UDI
510(k) Number
K120117 FDA UDI
FDA Product Code
KCT FDA UDI
GMDN Term
Sterilization container filter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 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

No

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: Sterilization container filter, single-use

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

Similar devices

Also classified as Sterilization container filter, single-use.

Cleared under the same submission

K120117 also covers:

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 2f89e784-dcc2-4975-8ad6-379a2e9de9e8 36 fields · synced Jun 8, 2026