Product code HNH— Ophthalmic
GELENDER VACUUM FIXATION RING SYS
- Classification name
- Ring, Ophthalmic (Flieringa)
- Device class
- Class 1
- Regulation
- 21 CFR 886.4350
- Advisory panel
- Ophthalmic
- Total cleared
- 7
- First cleared
- Most recent
Market context for product code HNH
FDA has cleared devices under product code HNH between 1984 and 1991, filed by 3 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
- 1991
- 1990
- 1986
- 1985
- 1984
Top applicants under product code HNH
Recent clearances under product code HNH
- K912268 — LANDERS NOTCHED VITRECTOMY LENS RING
- K912269 — LANDERS NOTCHED IRRIGATING VITRECTOMY LENS RING
- K912151 — LANDERS THREE STRUT VITRECTOMY LENS RING
- K902496 — LANDERS VITRECTOMY LENS RING W/INFUSION
- K863775 — RK VACUUM FIXATION RING SYSTEM
- K850991 — LANDERS VITRECTOMY LENS RING SYSTEMS
- K832912 — GELENDER VACUUM FIXATION RING SYS
Data sourced from openFDA. This site is unofficial and independent of the FDA.