Tubulitec Primer
FDA 510(k) K864052 · Dental Dimensions Supply Co.
510(k) numberK864052
Submission
- Device name
- Tubulitec Primer
- Applicant
- Dental Dimensions Supply Co.
Wantagh, NY, US - Received
- October 16, 1986
- Decision date
- December 5, 1986
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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|---|---|---|---|
| K262243 | Profisil FreeLBH · Traditional | Kettenbach GmbH & Co. KG | 09/03/2026SE |
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| K261404 | UltraEZLBH · Special | Ultradent Products, Inc. | 04/30/2026SE |
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| K250714 | FluoroDose VarnishLBH · Traditional | Centrix, Inc. | 11/21/2025SE |
| K243777 | Rennou Varnish (3% / Spearmint); Rennou Varnish (3% / Strawberry); Rennou Varnish (3%…LBH · Traditional | Theodent, LLC | 05/27/2025SE |
| K241489 | ReminGelLBH · Traditional | Inter-Med, Inc. | 01/08/2025SE |
| K241568 | CrystLCare PRO Biorestorative, Fluoride-PlusLBH · Traditional | GreenMark Biomedical, Inc. | 01/02/2025SE |
| K242913 | Jasmate® ToothpasteLBH · Traditional | Jasberry Healthcare Private Limited | 11/22/2024SE |
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Questions and answers
When was Tubulitec Primer cleared by the FDA?
Tubulitec Primer (K864052) received a 510(k) decision of Substantially Equivalent on December 5, 1986, 50 days after the submission was received.
What is the product code of K864052?
The FDA product code is LBH – Varnish, Cavity, a Class II (moderate risk) device regulated under 21 CFR 872.3260.