FDA Device Intelligence
HomeRichard Wolf GmbH › GREENLIGHT

GREENLIGHT

Richard Wolf GmbH · Model 8632027 · UDI-DI 04055207018118

FBO
10
510(k) clearances
275
Adverse events (1 deaths)
7
Recalls
22
Facilities

Description

INTERNAL SHEATH LASER THERAPY color code green, SL 209mm, oval, slanted distal end, stainless steel, continuous irrigation, compatible with outer sheath 8632026, working insert 8632914, attachment 8632264, and telescopes Ø 4mm, 12°/30°, with irrigation stopcock, quick-lock, reusable

Recalls

DateFirmReason
2023-09-25Aizu Olympus Co., Ltd.Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endo
2022-04-01Karl Storz EndoscopyFailure to achieve the expected six-log reduction in microorganisms following the disinfection process.
2022-04-01Karl Storz EndoscopyFailure to achieve the expected six-log reduction in microorganisms following the disinfection process.
2022-04-01Karl Storz EndoscopyFailure to achieve the expected six-log reduction in microorganisms following the disinfection process.
2022-04-01Karl Storz EndoscopyFailure to achieve the expected six-log reduction in microorganisms following the disinfection process.
2022-04-01Karl Storz EndoscopyFailure to achieve the expected six-log reduction in microorganisms following the disinfection process.
2020-04-13American Contract SystemsThe surgical gowns were manufactured in a facility that is not registered by the FDA.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.