510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K961418Substantially Equivalent

Osteomed Mss

Osteomed, Irving TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K961418 is the FDA 510(k) clearance record for OSTEOMED MSS, a class II device, cleared for Osteomed Corp. on under FDA product code DZL (Screw, Fixation, Intraosseous). FDA records list 73 510(k) clearances for Osteomed Corp., from to . As of , FDA records show no recalls naming K961418.

Clearance record

Decision date
Received
(196 days to decision)
Product code
DZL Screw, Fixation, Intraosseous
Regulation
21 CFR 872.4880
Device class
Class II
Review panel
Dental
Applicant
Osteomed Corp. 3150 Premier Dr., Irving TX
510(k) summary
Statement
Third party review
No

Clearances, product code DZL

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