FDA Device Intelligence
Home › Dynarex Corporation › Nasal Sponges Sterile

Nasal Sponges Sterile

Dynarex Corporation · Model 3168 · UDI-DI 00840117340206

EMX
10
510(k) clearances
103
Adverse events (2 deaths)
4
Recalls
51
Facilities

Description

Sterile-R, 3.14" x 1.18" x 0.59" (8.0 cm x 3.0 cm x 1.5 cm)

Recalls

DateFirmReason
2003-01-08Ultracell Medical TechnologiesSterility of the device is compromised
2003-01-08Ultracell Medical TechnologiesSterility of the device is compromised
2003-01-08Ultracell Medical TechnologiesSterility of the device is compromised
2003-01-08Ultracell Medical TechnologiesSterility of the device is compromised

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.