Atlas FDA

VOCO Profluorid Varnish + BioMin

FDA 510(k) clearance K252073 · decided 2026-05-01

Clearance details

K-number
K252073
Device name
VOCO Profluorid Varnish + BioMin
Applicant
Voco GmbH
Decision
Substantially Equivalent
Date received
2025-07-02
Decision date
2026-05-01
Days to decision
303 days
Clearance type
Traditional
Product code
LBH
Device class
2
Regulation number
872.3260
Medical specialty
Dental
Advisory committee
Dental
Location
Cuxhaven, DE
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Fluoride Varnish (Type A,Type C) (K253052)Nagy Oral Technology Qinhuangdao Co., Ltd.2026-06-11
UltraEZ (K261404)Ultradent Products, Inc.2026-04-30
APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste) (K260830)Sangi Co., Ltd.2026-03-18
FluoroDose Varnish (K250714)Centrix, Inc.2025-11-21
Rennou™ Varnish (3% / Spearmint); Rennou™ Varnish (3% / Strawberry); Rennou™ Varnish (3% / Cherry); Rennou™ Varnish (3% / Bubble Gum) (K243777)Theodent, LLC2025-05-27
ReminGel (K241489)Inter-Med, Inc.2025-01-08
CrystLCare™ PRO Biorestorative, Fluoride-Plus (K241568)GreenMark Biomedical, Inc.2025-01-02
Jasmate® Toothpaste (K242913)Jasberry Healthcare Private Limited2024-11-22
Papacarie Duo (K233768)Elevate Oral Care2024-07-18
ProMin Dental Desensitizing Gel (K231060)Belport Company, Inc., Gingi-Pak2024-06-13
Profisil Fluoride Varnish Combi pack (14801), Profisil Fluoride Varnish Normal pack mint (14802), Profisil Fluoride Varnish Normal pack berry (14804), Profisil Fluoride Varnish Normal pack unflavored (14806), Profisil Fluoride Varnish Sample pack (14800) (K230333)Kettenbach GmbH & Co. KG2023-07-24
Dental Desensitizer (K222891)Guangzhou Beogene Biotech Co., Ltd.2023-05-25

Recalls involving this device

No recalls on record reference this clearance.