510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K801686Substantially Equivalent

Spaceline Three Way Syringe

Pacific Dental Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K801686 is the FDA 510(k) clearance record for SPACELINE THREE WAY SYRINGE, a class I device, cleared for Pacific Dental Corp. on under FDA product code ECB (Unit, Syringe, Air And/Or Water). FDA records list 22 510(k) clearances for Pacific Dental Corp., from to . As of , FDA records show no recalls naming K801686.

Clearance record

Decision date
Received
(14 days to decision)
Product code
ECB Unit, Syringe, Air And/Or Water
Regulation
21 CFR 872.4565
Device class
Class I
Review panel
Dental
Applicant
Pacific Dental Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code ECB

Trailing 12 months

FDA records hold no clearances under product code ECB in the trailing twelve months.

FDA records show no clearances under product code ECB in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code ECB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260