REPLICA DENTAL COMPOSIT— 510(k) K771880

Substantially Equivalent

Hoyt Laboratories

FDA 510(k) clearance K771880 for REPLICA DENTAL COMPOSIT, Substantially Equivalent on 1977-10-20. Applicant: Hoyt Laboratories. Device class: 2.

Clearance details

Applicant: Hoyt Laboratories
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 1977-10-04
Decision date: 1977-10-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EBF

K262202 — Cerasmart Forte2026-09-10
K261695 — Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)2026-08-31
K261485 — Tetric plus Fill; Tetric plus Flow2026-07-01
K262228 — Transcend Bulk Fill Flowable Composite2026-07-01
K261246 — SRGC-062026-06-18

More clearances from Hoyt Laboratories

K820738 — LUSTRALLOY1982-04-09
K811154 — HOYT ECONO-TRAY1981-05-13
K810830 — HOYT COTTON ROLLS1981-04-14
K780834 — PREVI DENT PROPHYLAXIS MINT NDC1978-06-02
K771881 — REPLICA BONDING AGENT1977-11-09

Data sourced from openFDA. This site is unofficial and independent of the FDA.