Renamel® Microfill 6072B1

by Cosmedent, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberD7796072B11 UDI-DI	Date22 Sep 2017Listed	StatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Renamel® Microfill
Generic Name: Dental composite resin
Model / Ref / Catalog: 6072B1

Primary DI / UDI-DI: D7796072B11
510(k) Number: K854755
FDA Product Code: EBF
GMDN Term: Dental composite resin

Device Class: Class II
Regulation Number: 872.3690
GUDID distribution status: In Commercial Distribution

From the manufacturer

Manufacturer's product page: Renamel Microfill Dental Composite

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Properties

Single Use
Prescription Use
Lot / Batch Number
Expiration Date

Other properties (10)

Sterile: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No
Manufacturing Date: No