510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K901928Substantially Equivalent

Interpore Imz(castable)tub/scret Ret Rigid Attach

Interpore Intl., Rockville MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K901928 is the FDA 510(k) clearance record for INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACH, a class I device, cleared for Interpore Intl. on under FDA product code EGG (Attachment, Precision, All). FDA records list 25 510(k) clearances for Interpore Intl., from to . As of , FDA records show no recalls naming K901928.

Clearance record

Decision date
Received
(90 days to decision)
Product code
EGG Attachment, Precision, All
Regulation
21 CFR 872.3165
Device class
Class I
Review panel
Dental
Applicant
Interpore Intl. Aba Bioresearch, Rockville MD
Third party review
No

Clearances, product code EGG

Trailing 12 months

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

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