Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K090401Substantially Equivalent

Orthoss

Ed. Geistlich Soehne AG Fur Chemische Industrie, Washington DC / Traditional, Substantially Equivalent

K090401 is the FDA 510(k) clearance record for ORTHOSS, a class II device, cleared for Ed. Geistlich Soehne AG Fur Chemische Industrie on under FDA product code MQV (Filler, Bone Void, Calcium Compound). FDA records list 2 510(k) clearances for Ed. Geistlich Soehne AG Fur Chemische Industrie, from to . As of , FDA records show no recalls naming K090401.

Clearance record

Decision date
Received
(325 days to decision)
Product code
MQV Filler, Bone Void, Calcium Compound
Regulation
21 CFR 888.3045
Device class
Class II
Review panel
Orthopedic
Applicant
Ed. Geistlich Soehne AG Fur Chemische Industrie 1300 I St., NW, 11th Floor, Washington DC
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MQV

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