510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K003787Substantially Equivalent

Newtom Qr-Dvt 9000

Aperio Services, LLC, Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K003787 is the FDA 510(k) clearance record for NEWTOM QR-DVT 9000, a class II device, cleared for Aperio Services, LLC on under FDA product code OAS (X-Ray, Tomography, Computed, Dental). FDA's definition for product code OAS reads: "Produce cross-sectional diagnostic x-ray images of the intra-oral tissue and teeth". FDA records list 2 510(k) clearances for Aperio Services, LLC, from to . As of , FDA records show no recalls naming K003787.

Clearance record

Decision date
Received
(90 days to decision)
Product code
OAS X-Ray, Tomography, Computed, Dental
Regulation
21 CFR 892.1750
Device class
Class II
Review panel
Radiology
Applicant
Aperio Services, LLC 815 Connecticut Ave. NW, Washington DC
510(k) summary
Summary
Third party review
No

Clearances, product code OAS

Trailing 12 months
11 clearances under product code OAS in the twelve months to October 2026, November 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code OAS, trailing twelve months
MonthClearances
November 20252
December 20250
January 20260
February 20261
March 20262
April 20261
May 20261
June 20262
July 20261
August 20260
September 20261
October 20260