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510(k) Predicate Database
FDA 510(k) ClearanceGEI

SYNERJET PRO (SP-1002); InPhiuse (SP-1002); WOWJET (SP-1002)

FDA 510(k) K260397 · Hironic Co., Ltd.

Clearance details

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510(k) number
K260397
Device name
SYNERJET PRO (SP-1002); InPhiuse (SP-1002); WOWJET (SP-1002)
Applicant
Hironic Co., Ltd.
Product code
GEI
Decision
Substantially Equivalent
Decision date
Device class
Class 2
Regulation number
878.4400
Advisory committee
SU
Medical specialty
General, Plastic Surgery

Candidate predicate devices

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Other devices cleared under product code GEI form a screening cohort, not a predicate determination. Compare intended use, technological characteristics, performance evidence, labeling, and current legal-marketing status before selecting a predicate.

Candidate predicate devices for K260397
510(k)DeviceApplicantDecision date
K254196HARMONIC 1100 Shears (HAR1120); HARMONIC 1100 Shears (HAR1136)Ethicon Endo-Surgery, LLC
K261959Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Push Button Switch (0703-046-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Push Button Switch, Bulk Non-Sterile (0703-046-102);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Rocker Switch (0703-047-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Rocker Switch, Bulk Non-Sterile (0703-047-102)Stryker Instruments
K261070LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coatedCovidien, LLC
K254185Potenza PrimeJeisys Medical Incorporated
K262364Ellian Enigma RF DeviceEllian Corp
K253859Scarlet Pro (Scarlet Pro)VIOL Co., Ltd.
K252535Inno-Switch™ Laparoscopic InstrumentsTaiwan Surgical Corporation
K261179AlphaTriPart - Monopolar MIC InstrumentsGimmi GmbH
K253504Volnewmer™Classys, Inc.
K254056THUNDERBEAT 5 mm, 45 cm, Front-actuated Grip Type S (TB-0545FCS); THUNDERBEAT 5 mm, 35 cm, Front-actuated Grip Type S (TB-0535FCS); THUNDERBEAT 5 mm, 20 cm, Front-actuated Grip Type S (TB-0520FCS)Olympus Medical Systems Corp.
K251492Irrigation Tubing Bipolar Cord SetNew Deantronics Taiwan , Ltd.
K253484LUTRONIC GENIUSCynosure Lutronic Technology Corporation
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Building a 510(k) around this device type?

Assyro turns predicate research into a substantial-equivalence comparison and an eSTAR-ready 510(k) workflow, so predicate strategy, testing evidence, and labeling stay aligned before FDA review.

  • PubMed
  • ClinicalTrials.gov
  • FDA
  • Health Canada
  • EMA
  • ICH
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