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
K021702Substantially Equivalent

Cryobag, Model Cb

OriGen Biomedical, Inc., Austin TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K021702 is the FDA 510(k) clearance record for CRYOBAG, MODEL CB, cleared for Origen Biomedical, Inc. on under FDA product code LPZ (Container, Frozen Donor Tissue Storage). FDA records list 4 510(k) clearances for Origen Biomedical, Inc., from to . As of , FDA records show no recalls naming K021702.

Clearance record

Decision date
Received
(75 days to decision)
Product code
LPZ Container, Frozen Donor Tissue Storage
Device class
Unclassified
Review panel
Unknown
Applicant
Origen Biomedical, Inc. 9709-A Beck Cir., Austin TX
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LPZ

Trailing 12 months

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

FDA records show no clearances under product code LPZ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LPZ, 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