510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K140038Substantially Equivalent

Digimatch Orthodoc Robodoc Encore Surgical System

Curexo Technology Corporation, Melrose MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K140038 is the FDA 510(k) clearance record for DIGIMATCH ORTHODOC ROBODOC ENCORE SURGICAL SYSTEM, a class II device, cleared for Curexo Technology Corporation on under FDA product code OJP (Orthopedic Computer Controlled Surgical System). FDA's definition for product code OJP reads: "Pre-operative planning and intra-operative execution of surgical movements with robotically controlled end effectors under user supervision. Alternative to manual planning and broaching/reaming techniques for femoral canal preparation in...". FDA records list 2 510(k) clearances for Curexo Technology Corporation, from to . As of , FDA records show no recalls naming K140038.

Clearance record

Decision date
Received
(140 days to decision)
Product code
OJP Orthopedic Computer Controlled Surgical System
Regulation
21 CFR 882.4560
Device class
Class II
Review panel
Neurology
Applicant
Curexo Technology Corporation 32 Harrison St., Melrose MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code OJP

Trailing 12 months

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

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