Zimmer Biomet Korea Ltd. (foreign exporter, Seoul, KR): 8 new FDA device listings, incl. prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or

Zimmer Biomet Korea Ltd. (Seoul): 8 new FDA device listings, incl. prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or . Its amount of 8 is top-decile (91st percentile of 2,570 records). Dated 83 days ago, it serves as a historical benchmark. Score 55/100. As of 2026-10-28, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).

Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)

amount: 8 · 91th percentile of 2,570 DeviceEstablishmentPulse records · 8.0x the median

Free preview: all 15 published fields of this record are shown below. Locked: 116 related KR DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentZimmer Biomet Korea Ltd.
Owner / operatorZimmer Biomet APAC DFE
RoleForeign exporter
Establishment typesExport Device to the United States But Perform No Other Operation on Device
LocationSeoul, KR
New listings8
DevicesProsthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous Cemented, Osteophilic Finish; Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented; Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer; Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented; Prosthesis, Hip, Hemi-, Femoral, Metal; Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented; Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
Product codesMAY, JDI, LZO, KWZ, LPH, KWL, KWY, MEH
Device classesClass II
Medical specialtiesOrthopedic
Brand namesTaperloc Complete Hip Stems
First new listing2026-08-13
Latest new listing2026-08-13
FDA registration number3015542154
Registration expires2027-12-31
amount percentile91th of 2,570 (median 1, 8.0x median)
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL

  • Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
  • Record date: 2026-08-13
  • Data refreshed: 2026-10-28
  • Refunds on request within 14 days

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LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 28 Oct 2026 20:51:27 GMT

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Peer benchmark and outreach value: Zimmer Biomet Korea Ltd. and 117 KR peers

  • KR DeviceEstablishmentPulse records like this one: 117
  • Zimmer Biomet Korea Ltd.'s amount: 91st percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every KR peer: $23,400 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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55 / 100 Score

  • Class II or III devices: QMS and regulatory demands.
  • Several new listings at once.

What is the DeviceEstablishmentPulse record for Zimmer Biomet Korea Ltd. in Seoul?

Zimmer Biomet Korea Ltd. (Seoul, KR), a foreign exporter, added 8 FDA device listings on 2026-08-13.

How does Zimmer Biomet Korea Ltd. compare to other DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 8 is 8.0x the median of 1 across 2,570 records. It is 83 days old; check the official source for later updates before acting.

Zimmer Biomet Korea Ltd. vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Zimmer Biomet Korea Ltd.Seoul, KR891st2026-08-13
Mka Medikal Ic Ve Dis Ticaret Sanayi Limited SirketiCankaya Ankara, TR992nd2026-10-17
Optikal (Southgate) LtdBorehamwood, GB377th2026-10-13
Loudwater Trade Finance LtdLONDON England, GB377th2026-10-09

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DeviceEstablishmentPulse: Foreign exporter DeviceEstablishmentPulse: Foreign establishment

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From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.

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