Product code HNC— Ophthalmic
ASNIS GUIDED SCREW SYSTEMS
- Classification name
- Specula, Ophthalmic
- Device class
- Class 1
- Regulation
- 21 CFR 886.4350
- Advisory panel
- Ophthalmic
- Total cleared
- 11
- First cleared
- Most recent
Market context for product code HNC
FDA has cleared devices under product code HNC between 1976 and 2002, filed by 9 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
- 2002
- 1998
- 1996
- 1986
- 1984
- 1983
- 1980
- 1976
Top applicants under product code HNC
Recent clearances under product code HNC
- K022836 — STEPHENS DISPOSABLE SPECULUM
- K981235 — OCULOSTAT
- K964289 — EYE FIXATION SPECULUM
- K863989 — THORNTON TITANIUM SPECULUM (MODIFIED BARRAQUER)
- K863664 — OPHTHALMIC SURGICAL SPECULUM
- K843196 — VISITEC EYE SPECULUM
- K830430 — EYELID SPECULUM
- K801969 — ASNIS GUIDED SCREW SYSTEMS
- K760847 — FELDSTEIN BLEPHAROPLASTY CLIP SHARP P
- K760848 — FELDSTEIN BLEPHAROPLASTY CLIP RECTANGU
- K760849 — FELDSTEIN BLEPHAROSTOMY CLIP SQUARE
Data sourced from openFDA. This site is unofficial and independent of the FDA.