Home › Device types › EXX
Probe, Rectal, Non-Powered
FDA product code EXX · Class 1 · Gastroenterology, Urology
65
Registered devices
10
Adverse events
1
Recalls
0
510(k) clearances
Devices with this code
Gimmi — Gimmi GmbHMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftV. Mueller — STERIS CORPORATIONV. Mueller — STERIS CORPORATIONNovo Surgical Inc. — NOVO SURGICAL, INC.Novo Surgical Inc. — NOVO SURGICAL, INC.Marina Medical — MARINA MEDICAL INSTRUMENTS, INC.Marina Medical — MARINA MEDICAL INSTRUMENTS, INC.AESCULAP — AESCULAP, INC.GreenEgg — Endoglow, LLCNovo Surgical Inc. — NOVO SURGICAL, INC.Novo Surgical — NOVO SURGICAL, INC.Novo Surgical — NOVO SURGICAL, INC.AESCULAP — AESCULAP, INC.Medicon — Medicon eG. Chirurgiemechaniker-GenossenschaftV. Mueller — STERIS CORPORATIONIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONMarina Medical — MARINA MEDICAL INSTRUMENTS, INC.Novo Surgical — NOVO SURGICAL, INC.Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONV. Mueller — STERIS CORPORATIONMEDRAD® PRO-TEKT Endorectal Balloon — BAYER MEDICAL CARE INC.Marina Medical — MARINA MEDICAL INSTRUMENTS, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2009-04-09 | Marina Medical Instruments Inc. | Marina Medical, Sunrise, FL initiated recall of 46 different 350 series devices and 47 different 270 series products because the material used to manufacture th |
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