FDA Device Intelligence
HomeAESCULAP, INC. › AESCULAP

AESCULAP

AESCULAP, INC. · Model MA636R · UDI-DI 04046964589058

HNQ Prescription
10
510(k) clearances
109
Adverse events
4
Recalls
187
Facilities

Description

STEVENS TENOTOMY HOOK 5MM CVD 117MM

Recalls

DateFirmReason
2025-12-16Vortex Surgical Inc.There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination
2025-12-16Vortex Surgical Inc.There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.
2022-03-16Carl Zeiss Meditec AGHigh friction of the slider can cause the device to stick, or not move as intended.

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.