Master-Dent 10-920

by Dentonics, Inc.

Master-Dent 10-920 is a device made by Dentonics, Inc., cleared under FDA 510(k) K933543 on 1 Nov 1993 and listed in FDA GUDID since 16 Sep 2016 (UDI-DI 00816526020206), 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	Number00816526020206 UDI-DI	Date16 Sep 2016Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK933543	Date1 Nov 1993Decided	StatusActive

Official records

AccessGUDID record UDI-DI 00816526020206
FDA 510(k) database 510(k) number K933543

Across registries

2 registries list this device

FDA 510(k) K933543 decided 1 Nov 1993 Active
FDA GUDID UDI-DI 00816526020206 listed 16 Sep 2016 Listed

Timeline

2 dated events

1 Nov 1993 Cleared FDA 510(k) K933543
16 Sep 2016 Listed FDA GUDID 00816526020206

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Master-Dent
Generic name: Home-use dental cement
Model / reference: 10-920

Primary DI / UDI-DI: 00816526020206
510(k) Number: K933543
GMDN term: Home-use dental cement

GUDID distribution status: In Commercial Distribution

Other devices from Dentonics, Inc.

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Class II
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Not classified
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Master-Dent 18-125

Not classified

See all devices from Dentonics, Inc. →

Properties

Convenience kit
Lot / batch number
Expiration date

Other properties (12, all answered No)