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Symmetry Secto®

FDA UDI

Class II (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Secto® FDA UDI
Generic Name
Dissection sponge FDA UDI
Device Name
Secto® Dissector, Gauze, 5 mm, 2.5 cm Working Length, Single-Use Tip, (10/bx) FDA UDI
Model / Reference
SG5 FDA UDI
Description
Secto® Dissector, Gauze, 5 mm, 2.5 cm Working Length, Single-Use Tip, (10/bx) FDA UDI

Identifiers

Primary DI / UDI-DI
10887482155261 FDA UDI
510(k) Number
K982428 FDA UDI
FDA Product Code
HET FDA UDI
GMDN Term
Dissection sponge FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1720 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Width — 5 Millimeter FDA UDI
Length — 2.5 Centimeter FDA UDI

Category: Dissection sponge

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

Similar devices

Also classified as Dissection sponge.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a5b054ba-9ebe-40fc-bf01-cc30baf6b5fe 36 fields · synced May 30, 2026