510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K944848Substantially Equivalent

The Vivacare T.p.s. Probe

Rms Div., Amherst NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K944848 is the FDA 510(k) clearance record for THE VIVACARE T.P.S. PROBE, a class I device, cleared for Rms Div. on under FDA product code EIX (Probe, Periodontic). FDA records list 10 510(k) clearances for Rms Div., from to . As of , FDA records show no recalls naming K944848.

Clearance record

Decision date
Received
(75 days to decision)
Product code
EIX Probe, Periodontic
Regulation
21 CFR 872.4565
Device class
Class I
Review panel
Dental
Applicant
Rms Div. 175 Pineview Dr., Amherst NY
510(k) summary
Statement
Third party review
No

Clearances, product code EIX

Trailing 12 months

FDA records hold no clearances under product code EIX in the trailing twelve months.

FDA records show no clearances under product code EIX in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EIX, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260