FDA Device Intelligence
HomeTHD SPA › THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope

THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope

THD SPA · Model Bevelled Anoscope Medium Sterile · UDI-DI 08033737710135

GCPFER Prescription
10
510(k) clearances
697
Adverse events
5
Recalls
16
Facilities

Description

The THD anoscope is a disposable medical device deemed for investigation of the anal canal. Available with truncated or beveled tip.

Recalls

DateFirmReason
2025-11-11Olympus Corporation of the AmericasComplaints of the ceramic tip of the resection sheath breaking have been received.
2024-09-13Olympus Corporation of the AmericasOlympus is removing the statement of compatibility with a GreenLight Laser for BPH therapy from the Instruction for Use (IFU) due to the potential for a damaged tip during use of a
2024-09-13Olympus Corporation of the AmericasProduct being removed due to incompatibility when used in conjunction with a GreenLight Laser for BPH therapy which could damage the tip of the device.
2017-08-18Olympus Corporation of the AmericasOlympus has received complaints about fragments of adhesive which detached from inside the working channel of the referenced products. Cracking, chipping, missing pieces, and delam
2017-04-19Olympus Corporation of the AmericasLoop wires breaking at the distal end of the Monopolar HF Resection Electrodes.

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.