510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K251255Substantially Equivalent

LymphaTech Mobile 3D Measuring Tool

Lymphatech, Atlanta GA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K251255 is the FDA 510(k) clearance record for LymphaTech Mobile 3D Measuring Tool, a class I device, cleared for Lymphatech, Inc. on under FDA product code SFG (Camera, Surgical, Measurement). FDA's definition for product code SFG reads: "An adjunctive tool to measure and record a body part’s physical data, such as diameter, surface area, volume, and perimeter/circumference. The device does not provide a diagnosis or therapy". FDA records list one 510(k) clearance for Lymphatech, Inc. As of , FDA records show no recalls naming K251255.

Clearance record

Decision date
Received
(90 days to decision)
Product code
SFG Camera, Surgical, Measurement
Regulation
21 CFR 878.4160
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Lymphatech, Inc. 976 Brady Ave. NW, Atlanta GA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code SFG

Trailing 12 months

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

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