Home › AMBLER SURGICAL CORP. › Ambler Surgical
Ambler Surgical
AMBLER SURGICAL CORP. · Model Guyton-Park lid speculum · UDI-DI 00190660178956
HNC
Prescription
10
510(k) clearances
21
Adverse events
1
Recalls
190
Facilities
Description
Guyton-Park lid speculum, 3 3/8'', adult size, 14.0mm fenestrated blades with suture posts and canthus bar, 38.0mm blade spread, nasal approach
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
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 docsData 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.
