Super-Slide III Instrument Case 7329-90M

by Koros USA, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10840199501684 UDI-DI	Date28 Jun 2021Listed	StatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Super-Slide III Instrument Case
Generic Name: Surgical retractor/retraction system blade, reusable
Model / Ref / Catalog: 7329-90M

Primary DI / UDI-DI: 10840199501684
510(k) Number: K881160
FDA Product Code: GZT
GMDN Term: Surgical retractor/retraction system blade, reusable

Device Class: Class II
Regulation Number: 882.4800
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

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Properties

Prescription Use
Lot / Batch Number
Serial Number

Other properties (11)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Expiration Date: No
Manufacturing Date: No