HomeUSAPECA LABS, INC.

PECA LABS, INC.

USA · Pittsburgh
✓ Record-verifiedregistrations found in 1 markets

This company has registrations in United States — 1 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
2listed device types
Class I 0Class II 2Class III 0
plus 6 registration records and 5 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
pendingnot queried
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States6 registration records, 5 510(k), 0 PMA
Manufacturer names merged into this page: PECA LABS, INC.

Company information

Country
USA
City
Pittsburgh

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

12018 · K180957
12019 · K183613
12020 · K202471
12022 · K221628
12024 · K233783

FDA listed device types

Prosthesis, Vascular Graft, Of 6mm And Greater Diameter 1Prosthesis, Vascular Graft, Of Less Then 6mm Diameter 1

Registration details (sample)

MarketIdentifierNameClass / date
USK233783exGraft ePTFE Vascular Grafts, exGraft Carbon ePTFE Vascular Grafts2024-01-17
USK221628exGraft, exGraft Carbon2022-08-04
USK202471exGraft ePTFE Vascular Graft, exGraft Carbon ePTFE Vascular Graft2020-12-11

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