Na 698328874

by Depuy Spine, Inc. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10705034231822 UDI-DI	Date11 Nov 2016Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Generic Name: Manual orthopaedic bender, reusable
Model / Ref / Catalog: 698328874

Primary DI / UDI-DI: 10705034231822
FDA Product Code: HXW
GMDN Term: Manual orthopaedic bender, reusable

Device Class: Class I
Regulation Number: 888.4540
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

Other devices from Depuy Spine, Inc.

N/A 698344998

Class I
N/A 698345075

Class I
N/A 698345076

Class I
N/A 698345077

Class I
N/A 698345078

Class I
N/A 698345079

Class I

See all devices from Depuy Spine, Inc. →

Properties

Prescription Use
Premarket Exempt
Lot / Batch 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
Serial Number: No
Expiration Date: No
Manufacturing Date: No