Massad MAUD2IO4

by Cmp Industries LLC

Massad MAUD2IO4 is a Class II device made by Cmp Industries LLC, cleared under FDA 510(k) K101029 on 16 Aug 2010 and listed in FDA GUDID since 21 Dec 2018 (UDI-DI M482MAUD2IO40), active as of 23 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 23 Oct 2026

Documents

FDA submission, from GUDID

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberM482MAUD2IO40 UDI-DI	Date21 Dec 2018Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK101029	Date16 Aug 2010Decided	StatusActive

Official records

FDA 510(k) database 510(k) number K101029

Across registries

2 registries list this device

FDA 510(k) K101029 decided 16 Aug 2010 Active
FDA GUDID UDI-DI M482MAUD2IO40 listed 21 Dec 2018 Listed

Timeline

2 dated events

16 Aug 2010 Cleared FDA 510(k) K101029
21 Dec 2018 Listed FDA GUDID M482MAUD2IO40

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Massad
Generic name: Resin artificial teeth
Model / reference: MAUD2IO4

Primary DI / UDI-DI: M482MAUD2IO40
510(k) Number: K101029
FDA product code: ELM
GMDN term: Resin artificial teeth

Device class: Class II
Regulation number: 872.3590
GUDID distribution status: In Commercial Distribution

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Properties

Single use
Prescription use
Lot / batch number

Other properties (12, all answered No)