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FDA 510(k)

G-FLOSS & G-FLOSS II

K-Number: K911701 · 1991-05-15

Decision Date1991-05-15
Product CodeJES
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

G-FLOSS & G-FLOSS II is the device name listed in this FDA 510(k) record. The listed applicant is Implant Innovations International, Inc.. It received FDA 510(k) clearance on 1991-05-15 under 510(k) number K911701. The device is classified under product code JES. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the G-FLOSS & G-FLOSS II?

G-FLOSS & G-FLOSS II is a medical device that received FDA 510(k) clearance on 1991-05-15. The listed applicant is Implant Innovations International, Inc.. The 510(k) number is K911701.

When did G-FLOSS & G-FLOSS II receive FDA 510(k) clearance?

G-FLOSS & G-FLOSS II received FDA 510(k) clearance on 1991-05-15, under 510(k) number K911701.

Who is the listed applicant for G-FLOSS & G-FLOSS II?

The FDA 510(k) record lists Implant Innovations International, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for G-FLOSS & G-FLOSS II?

The FDA product code for G-FLOSS & G-FLOSS II is JES.

Related Clinical Trials

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.

Other records listing Implant Innovations International, Inc. 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.

View all 18 devices →

Related Devices (Code: JES)

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.

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.

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