510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K000894Substantially Equivalent

C&b Resin Plus Powder/liquid, Models Retemp A2, A3, A3.5, Cl, Retemp B2, B3, C2, D3, Wh, Retemp Mo

Dental Ventures of America, Inc., Corona CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K000894 is the FDA 510(k) clearance record for C&B RESIN PLUS POWDER/LIQUID, MODELS RETEMP A2, A3, A3.5, CL, RETEMP B2, B3, C2, D3, WH, RETEMP MO, a class II device, cleared for Dental Ventures of America, Inc. on under FDA product code EBG (Crown And Bridge, Temporary, Resin). FDA records list 3 510(k) clearances for Dental Ventures of America, Inc., from to . As of , FDA records show no recalls naming K000894.

Clearance record

Decision date
Received
(60 days to decision)
Product code
EBG Crown And Bridge, Temporary, Resin
Regulation
21 CFR 872.3770
Device class
Class II
Review panel
Dental
Applicant
Dental Ventures of America, Inc. 217 Lewis Ct., Corona CA
510(k) summary
Statement
Third party review
No

Clearances, product code EBG

Trailing 12 months
2 clearances under product code EBG in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code EBG, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260