510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K130763Substantially Equivalent

Beacon Tissue Marker

Scion Medical Technologies, LLC, Sauk Centre MN / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K130763 is the FDA 510(k) clearance record for BEACON TISSUE MARKER, a class II device, cleared for Scion Medical Technologies, LLC on under FDA product code NEU (Marker, Radiographic, Implantable). FDA records list 6 510(k) clearances for Scion Medical Technologies, LLC, from to . As of , FDA records show no recalls naming K130763.

Clearance record

Decision date
Received
(49 days to decision)
Product code
NEU Marker, Radiographic, Implantable
Regulation
21 CFR 878.4300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Scion Medical Technologies, LLC 23879 Blue Spruce Rd., Sauk Centre MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NEU

Trailing 12 months
4 clearances under product code NEU in the twelve months to October 2026, December 2025 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code NEU, trailing twelve months
MonthClearances
November 20250
December 20253
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260