N-Force Blue IN050-5

N-Force Blue IN050-5 is a Class II device made by Etex Corp., cleared under FDA 510(k) K062630 on 28 Jun 2007 and listed in FDA GUDID since 28 Jan 2019 (UDI-DI 00889024563261), active as of 22 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

FDA submission, from GUDID

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	Number00889024563261 UDI-DI	Date28 Jan 2019Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK062630	Date28 Jun 2007Decided	StatusActive

Official records

AccessGUDID record UDI-DI 00889024563261
FDA 510(k) database 510(k) number K062630

Across registries

2 registries list this device

FDA 510(k) K062630 decided 28 Jun 2007 Active
FDA GUDID UDI-DI 00889024563261 listed 28 Jan 2019 Listed

Timeline

2 dated events

28 Jun 2007 Cleared FDA 510(k) K062630
28 Jan 2019 Listed FDA GUDID 00889024563261

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: N-Force Blue
Generic name: Synthetic bone graft
Model / Ref / Catalog: IN050-5

Primary DI / UDI-DI: 00889024563261
510(k) Number: K062630
FDA product code: MQV
GMDN term: Synthetic bone graft

Device class: Class II
Regulation number: 888.3045
GUDID distribution status: In Commercial Distribution

Similar devices in this category

Other devices filed under Synthetic bone graft.

Other devices from Etex Corp.

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Properties

Supplied sterile
Single use
Implantable
Prescription use
Manufacturing date

Other properties (10, all answered No)