510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K022425Substantially Equivalent

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Altatec Biotechnologies N.A., Inc., Potomac MD / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K022425 is the FDA 510(k) clearance record for SCREWLINE, a class II device, cleared for Altatec Biotechnologies N.A., Inc. on under FDA product code DZE (Implant, Endosseous, Root-Form). FDA records list one 510(k) clearance for Altatec Biotechnologies N.A., Inc. As of , FDA records show no recalls naming K022425.

Clearance record

Decision date
Received
(21 days to decision)
Product code
DZE Implant, Endosseous, Root-Form
Regulation
21 CFR 872.3640
Device class
Class II
Review panel
Dental
Applicant
Altatec Biotechnologies N.A., Inc. 9229 Cranford Dr., Potomac MD
510(k) summary
Statement
Third party review
No

Clearances, product code DZE

Trailing 12 months
19 clearances under product code DZE in the twelve months to October 2026, December 2025 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code DZE, trailing twelve months
MonthClearances
November 20251
December 20254
January 20261
February 20262
March 20264
April 20260
May 20261
June 20264
July 20260
August 20261
September 20261
October 20260