ReNew 6152

by Microline Surgical, Inc.

ReNew 6152 is a Class II device made by Microline Surgical, Inc., listed in FDA GUDID since 13 Nov 2017 (UDI-DI 00811099010890), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00811099010890 UDI-DI	Date13 Nov 2017Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00811099010890

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: ReNew
Generic name: Endoscopic electrosurgical electrode, monopolar, single-use
Model / Ref / Catalog: 6152

Primary DI / UDI-DI: 00811099010890
FDA product code: GEI
GMDN term: Endoscopic electrosurgical electrode, monopolar, single-use

Device class: Class II
Regulation number: 878.4400
GUDID distribution status: In Commercial Distribution

Other devices from Microline Surgical, Inc.

ReNew 3412

Class II
ReNew 3362

Class II
ReNew 3946

Class II
ReNew 3411

Class II

See all devices from Microline Surgical, Inc. →

Properties

Supplied sterile
Single use
Prescription use
Lot / batch number
Expiration date

Other properties (10, all answered No)