510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K972308Substantially Equivalent

Mednext 1000 Drill

Mednext, Inc., West Palm Beach FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K972308 is the FDA 510(k) clearance record for MEDNEXT 1000 DRILL, a class I device, cleared for Mednext, Inc. on under FDA product code GEY (Motor, Surgical Instrument, Ac-Powered). FDA records list 7 510(k) clearances for Mednext, Inc., from to . As of , FDA records show no recalls naming K972308.

Clearance record

Decision date
Received
(61 days to decision)
Product code
GEY Motor, Surgical Instrument, Ac-Powered
Regulation
21 CFR 878.4820
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Mednext, Inc. 5490 Dexter Way, West Palm Beach FL
510(k) summary
Statement
Third party review
No

Clearances, product code GEY

Trailing 12 months

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

FDA records show no clearances under product code GEY in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GEY, 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