Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

joimax Electrosurgical Instruments

K-Number: K161378 · 2016-11-02

ApplicantJoimax GmbH
Decision Date2016-11-02
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

joimax Electrosurgical Instruments is the device name listed in this FDA 510(k) record. The listed applicant is Joimax GmbH. It received FDA 510(k) clearance on 2016-11-02 under 510(k) number K161378. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the joimax Electrosurgical Instruments?

joimax Electrosurgical Instruments is a medical device that received FDA 510(k) clearance on 2016-11-02. The listed applicant is Joimax GmbH. The 510(k) number is K161378.

When did joimax Electrosurgical Instruments receive FDA 510(k) clearance?

joimax Electrosurgical Instruments received FDA 510(k) clearance on 2016-11-02, under 510(k) number K161378.

Who is the listed applicant for joimax Electrosurgical Instruments?

The FDA 510(k) record lists Joimax GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for joimax Electrosurgical Instruments?

The FDA product code for joimax Electrosurgical Instruments is GEI.

Other records listing Joimax GmbH as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K203014EndoLIF Delta-Cage and DoubleWedge-CageK192663Joimax Intracs SystemK192680Percusys® Plus Pedicle Screw SystemK170358joimax Endovapor 2

Related Devices (Code: GEI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261179AlphaTriPart - Monopolar MIC InstrumentsGimmi GmbHK253504Volnewmer™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.K253484LUTRONIC GENIUSCynosure Lutronic Technology CorporationK251492Irrigation Tubing Bipolar Cord SetNew Deantronics Taiwan , Ltd.K260636Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coatingStryker Sustainability Solutions

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑