Product code MOE— Ophthalmic
COLLAGEN SHIELD FOR ACUTE CARE
- Classification name
- Collagen Corneal Shield
- Device class
- Class 1
- Regulation
- 21 CFR 886.4750
- Advisory panel
- Ophthalmic
- Total cleared
- 19
- First cleared
- Most recent
Market context for product code MOE
FDA has cleared devices under product code MOE between 1987 and 1995, filed by 8 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1995
- 1992
- 1991
- 1990
- 1989
- 1988
- 1987
Top applicants under product code MOE
Recent clearances under product code MOE
- K944872 — BIO-COR COLLAGEN CORNEAL SHIELD
- K915861 — MEDILENS-CS CORNEAL SHIELD
- K914529 — SOFTSHIELD(TM) 12, 24, 72 COLLAGEN CORNEAL SHIELDS
- K913148 — COLLAGEN SHIELD FOR ACUTE CARE
- K905825 — COLLAGEN SHIELD, VARIOUS MODELS
- K902558 — COLLAGEN SHIELD FOR ACUTE CARE
- K901880 — MEDILENS(TM) CORNEAL SHIELD
- K896449 — IM COLLAGEN SHIELD
- K884962 — ADDIT. INDICATIONS FOR BIO-COR EXT COLLAGEN CORNEA
- K885015 — COI 72 HR COLLAGEN SHIELD
- K884960 — ADDIT. INDICATION FOR FYODOROV COLLAGEN CORNEAL
- K884961 — ADDIT. INDICATIONS FOR BIO-COR II COLLAGEN CORNEAL
- K885016 — COI 24 HR COLLAGEN SHIELD
- K884363 — LABELING CHANGES TO BIO-COR II COLLANGEN CORNEAL
- K884364 — LABELING CHANGES TO BIO-COR EXT COLLANGEN CORNEAL
- K882762 — COLLAGEN SHIELD
- K874224 — BIO-COR II COLLAGEN CORNEAL SHIELD
- K874225 — BIO-COR EXT COLLAGEN CORNEAL SHIELD
- K862315 — FYODOROV COLLAGEN CORNEAL SHIELD
Data sourced from openFDA. This site is unofficial and independent of the FDA.