510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K002932Substantially Equivalent

Phacogard

Syntec, Inc., Winfield MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K002932 is the FDA 510(k) clearance record for PHACOGARD, a class II device, cleared for Syntec, Inc. on under FDA product code HQC (Unit, Phacofragmentation). FDA records list 3 510(k) clearances for Syntec, Inc., from to . As of , FDA records show no recalls naming K002932.

Clearance record

Decision date
Received
(106 days to decision)
Product code
HQC Unit, Phacofragmentation
Regulation
21 CFR 886.4670
Device class
Class II
Review panel
Ophthalmic
Applicant
Syntec, Inc. 733 Mansion Rd., Winfield MO
510(k) summary
Statement
Third party review
No

Clearances, product code HQC

Trailing 12 months
3 clearances under product code HQC in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HQC, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20261
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260